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This page only Certain Product LOTS are being Recalled as part of the July 8, 2010, June 15, 2010 and the January 15, 2010 recalls of Over-the-Counter (OTC) products.

To find out if your product has been recalled as part of the July 8, 2010, June 15, 2010 and the January 15, 2010 recalls of Over-the-Counter (OTC) products, please enter its lot # in any of the boxes below. Click here for information on other recalls.

If your product LOT # is recalled, you will be taken to the product details on this page.

If the product lot # you enter is not part of the July 8, 2010, June 15, 2010 and the January 15, 2010 recalls of Over-the-Counter (OTC) products, you will get a message letting you know. Click here for information on other recalls.

NOTE: Please be sure to enter both numeric and alphabetic characters correctly to find the exact LOT #. If you are unsure of whether a character is numeric (ex. the number 0) or alphabetic (ex. the letter O), please call our Consumer Care Center at 1-888-222-6036 and someone will help you verify.

Only Certain Product LOTS are being Recalled as part of the July 8, 2010, June 15, 2010 and the January 15, 2010 recalls of Over-the-Counter (OTC) products.

To find out if your BENADRYL® product has been recalled, please enter its LOT # here

If your BENADRYL® product LOT # is recalled, you will be taken to the product details on this page.

If the product lot # you enter is not part of the July 8, 2010, June 15, 2010 and the January 15, 2010 recalls of Over-the-Counter (OTC) products, you will get a message letting you know. Click here for information on other recalls.

NOTE: Please be sure to enter both numeric and alphabetic characters correctly to find the exact LOT #. If you are unsure of whether a character is numeric (ex. the number 0) or alphabetic (ex. the letter O), please call our Consumer Care Center at 1-888-222-6036 and someone will help you verify.


Below you will find more details on specific products that are recalled. To find out if you have a product that is affected, please locate the NDC number and the lot number of the product you have. This information can be found on the box that the product was sold in and on the actual bottle itself. If you need help with finding this information, please call our Consumer Care Center at 1-888-222-6036.

Click here for information on other recalls.

Recall information on certain product lots of BENADRYL® ALLERGY TABLET™

Product Description:
BENADRYL® ALLERGY ULTRATAB™ 100 COUNT

NDC Code #
50580-226-10

UPC # 312547170338
LOT #s

AJA008

ADA194

ABA022

ABA264

ABA567

ABA574

Product Description:
BENADRYL® ALLERGY TABLET 148 COUNT

NDC Code #
50580-226-14

UPC # 300450226143
LOT #s

AAA422

ABA392

AJA094

ALA034

Go to Benadryl.com for more information or click here to find a store near you that has the product you are looking for.


Only Certain Product LOTS are being Recalled as part of the July 8, 2010, June 15, 2010 and the January 15, 2010 recalls of Over-the-Counter (OTC) products.

To find out if your TYLENOL® product has been recalled, please enter its LOT # here

If your TYLENOL® product LOT # is recalled, you will be taken to the product details on this page.

If the product lot # you enter is not part of the July 8, 2010, June 15, 2010 and the January 15, 2010 recalls of Over-the-Counter (OTC) products, you will get a message letting you know. Click here for information on other recalls.

NOTE: Please be sure to enter both numeric and alphabetic characters correctly to find the exact LOT #. If you are unsure of whether a character is numeric (ex. the number 0) or alphabetic (ex. the letter O), please call our Consumer Care Center at 1-888-222-6036 and someone will help you verify.


Below you will find more details on specific products that are recalled. To find out if you have a product that is affected, please locate the NDC number and the lot number of the product you have. This information can be found on the box that the product was sold in and on the actual bottle itself. If you need help with finding this information, please call our Consumer Care Center at 1-888-222-6036.

Click here for information on other recalls.

Product Description:
TYLENOL® EXTRA STRENGTH CAPLETS 325 COUNT

NDC Code #
50580-449-32

UPC #300450444325
LOT #s

SPA005

SPA058

SFA295 09BMC018
09CMC048 09FMC082
09FMC084 AAA405
ADA014 ADA087
ADA270 ADA271
ADA417 AEA348
AFA102 AJA045
ALA028 SFA179
SFA237 SFA295
SHA002 SJA025
SJA189 SJA232
SLA004 SLA160
SLA296 SMA173
SMA174 SSA055
SPA038 SPA386

Product Description:
TYLENOL® EXTRA STRENGTH CAPLET 100+25CT

NDC Code #
50580-449-00

UPC #300450449009
LOT #s

SDA203

SHA035

Product Description:
TYLENOL® EXTRA STRENGTH CAPLET 100CT

NDC Code #
50580-449-09

UPC #300450449092
LOT #s

AMA008

SSA013

SSA150  

Product Description:
TYLENOL® EXTRA STRENGTH CAPLET 150+50CT

NDC Code #
50580-449-46

UPC #300450449467
LOT #s

SFA071

 

   

Product Description:
TYLENOL® EXTRA STRENGTH CAPLET 150CT

NDC Code #
50580-449-23

UPC #300450449238
LOT #s

AAA419

SEA199

SPA007  

Product Description:
TYLENOL® EXTRA STRENGTH CAPLET 225CT

NDC Code #
50580-449-27

UPC #300450444271
LOT #s

SSA011

 

Product Description:
TYLENOL® EXTRA STRENGTH CAPLET 24+12CT

NDC Code #
50580-449-31

UPC #300450444318
LOT #s

ABA565

AHA040

AJA028  

Product Description:
TYLENOL® EXTRA STRENGTH CAPLET 24CT

NDC Code #
50580-449-05

UPC #300450449054
LOT #s

AAA408

ABA169

ABA568 ADA192
AHA048 AJA145

Product Description:
TYLENOL® EXTRA STRENGTH CAPLET 50+25CT

NDC Code #
50580-449-75

UPC #300450444752
LOT #s

ACA599

ACA755

Product Description:
TYLENOL® EXTRA STRENGTH CAPLET 50CT

NDC Code #
50580-449-07

UPC #300450449078
LOT #s

AJA021

AFA018

AFA176 AFA325
AHA072 AEA206

Product Description:
TYLENOL® EXTRA STRENGTH CAPLET 50CT

NDC Code #
50580-449-06

UPC #300450444530
LOT #s

ABA168

 

Product Description:
TYLENOL® EXTRA STRENGTH CAPLET 50CT

NDC Code #
50580-451-50

UPC #350580451502
LOT #s

24862

24881

24901 24970
25994 26054
26213 26305
26356 26377
26515 26541

Product Description:
TYLENOL® EXTRA STRENGTH COOL CAPLET 100CT

NDC Code #
50580-710-10

UPC #300450444103
LOT #s

ALA249

 

Product Description:
TYLENOL® EXTRA STRENGTH COOL CAPLET 50CT

NDC Code #
50580-710-50

UPC #300450444509
LOT #s

ABA029

ACA563

ADA190 AHA081
AJA095 AJA175

Product Description:
TYLENOL® EXTRA STRENGTH EZ TAB 24CT

NDC Code #
50580-422-24

UPC #300450422248
LOT #s

ABA154

ADA193

AFA243 AHA039

Product Description:
TYLENOL® EXTRA STRENGTH EZ TAB 50+25CT

NDC Code #
50580-422-75

UPC #300450422750
LOT #s

ACA562

ACA743

ALA173  

Product Description:
TYLENOL® EXTRA STRENGTH EZ TAB 225CT

NDC Code #
50580-422-37

UPC #300450422378
LOT #s

ASA206

 

Product Description:
TYLENOL® EXTRA STRENGTH EZ TAB 50CT

NDC Code #
50580-422-50

UPC #300450422507
LOT #s

ADA013

AEA259

AHA091 AJA010
AJA123 ABA005

Product Description:
TYLENOL® EXTRA STRENGTH COOLCPT 24CT

NDC Code #
50580-710-24

UPC #300450444240
LOT #s

ABA566

 

Product Description:
TYLENOL® EXTRA STRENGTH CAPLET 24+12CT

NDC Code #
50580-422-50

UPC #300450444318
LOT #s

ACA025

 

Product Description:
TYLENOL® EXTRA STRENGTH RAPID RELEASE GELCAP 100+20CT

NDC Code #
50580-488-20

UPC #300450488176
LOT #s

ALA253

AMA015

Product Description:
TYLENOL® EXTRA STRENGTH RAPID RELEASE GELCAP 150CT

NDC Code #
50580-488-15

UPC #300450488152
LOT #s

ASA015

 

Product Description:
TYLENOL® EXTRA STRENGTH RAPID RELEASE GELCAP 24CT

NDC Code #
50580-488-24

UPC #300450488244
LOT #s

ABA020

ABA371

ADA280 AHA082
ACA024  

Product Description:
TYLENOL® EXTRA STRENGTH RAPID RELEASE GELCAP 290CT

NDC Code #
50580-488-29

UPC #300450488299
LOT #s

SEA191

SEA192

SFA025 SFA026
SFA136 SLA052
SLA198  

Product Description:
TYLENOL® EXTRA STRENGTH RAPID RELEASE GELCAP 290CT

NDC Code #
50580-488-29

UPC #300450488213
LOT #s

09AMC008 AAA049
AAA360 ADA022
ADA178 ADA272
ADA482 AEA194
AFA010 AFA292
AHA035 AHA089
AJA167 ALA095
ALA096 SFA296
SHA039 SHA234
SLA270 SMA236
SPA037 SPA357
SSA019 SSA030
SSA054  

Product Description:
TYLENOL® EXTRA STRENGTH RAPID RELEASE GELCAP 50CT

NDC Code #
50580-488-50

UPC #300450488503
LOT #s

ACA451

AEA061

AEA244 AFA103
AFA240 AHA046
AHA080 AJA040
AJA041 ASA202

Product Description:
TYLENOL® EXTRA STRENGTH RAPID RELEASE GELCAPS 225CT

NDC Code #
50580-488-25

UPC #300450488251
LOT #s

AJA119

 

Product Description:
TYLENOL® EXTRA STRENGTH TABLET 60CT

NDC Code #
50580-499-68

UPC #300450499684
LOT #s

AEA243

 

Product Description:
TYLENOL® REGULAR STRENGTH CAPLET 50CT

NDC Code #
50580-501-50

UPC #350580501504
LOT #s

24777

24900
24971 25971
26019 26133
26271 26422
26482 26521

Product Description:
TYLENOL® REGULAR STRENGTH TABLET 100CT

NDC Code #
50580-496-60

UPC #300450496607
LOT #s

ABA148

ABA266
ABA373 ACA432
AFA101 AHA070
AJA009 ALA099
AMA018  

Product Description:
TYLENOL® 8 HOUR CAPLET 100CT

NDC Code #
50580-297-10

UPC #300450297112
LOT #s

ACM037

AFM351
AHM316 AHM376
AHM422 ALM388
ALM458 AMM368
AMM435  

Product Description:
TYLENOL® 8 HOUR CAPLET 24CT

NDC Code #
50580-297-24

UPC #300450297242
LOT #s

ADM032

 
   
   
   

Product Description:
TYLENOL® 8 HOUR CAPLET 24CT

NDC Code #
50580-297-24

UPC #300450297266
LOT #s

ASM379

AMM322
ALM325 AEM105
AEM087 ADM031
ACM056  

Product Description:
TYLENOL® ARTHRITIS CAPLET 150CT

NDC Code #
50580-112-15

UPC #300450838155
LOT #s

09GMC101

ASA065
ASA304  

Product Description:
TYLENOL® ARTHRITIS CAPLET 225CT

NDC Code #
50580-112-37

UPC #300450838377
LOT #s

07BMC009

07EMC027
09EMC073 09HMC108
ASA088 ASA119
ASA293  

Product Description:
TYLENOL® ARTHRITIS CAPLET 290CT

NDC Code #
50580-122-29

UPC #300450838292
LOT #s

AEA180

AHA076
AHA077 AJA019
AJA116 AJA117
ALA029 AMA025
AMA270 APA011
APA214 APA266

Product Description:
TYLENOL® ARTHRITIS CAPLET 50CT

NDC Code #
50580-112-50

UPC #300450838506
LOT #s

08KMC123

09DMC066

Product Description:
TYLENOL® ARTHRITIS GELTAB 20CT

NDC Code #
50580-292-20

UPC #300450292209
LOT #s

09BMC031

 

Product Description:
TYLENOL® ARTHRITIS GELTAB 40CT

NDC Code #
50580-292-40

UPC #300450292407
LOT #s

08KMC130

09BMC024

Product Description:
TYLENOL® ARTHRITIS GELTAB 80CT

NDC Code #
50580-292-80

UPC #300450292803
LOT #s

ALM345

APM305
APM419 ASM357

Product Description:
TYLENOL® ARTHRITIS CAPLET 100CT - (DECEMBER 2009 RECALL)

NDC Code #
50580-112-10

UPC #300450838216
LOT #s

07CMC011

07DMC022

07DMC024

07FMC032

07FMC033

07GMC038

07GMC039

07HMC045

07HMC051

07HMC053

07JMC064

07JMC069

07JMC070

07JMC071

07XMC055

07XMC058

07XMC062

08AMC002

08AMC005

08CMC026

08DMC029

08EMC037

08EMC039

08FMC044

08FMC045

08GMC050

08GMC053

08GMC063

08GMC065

08JMC103

08JMC109

08JMC110

08JMC111

08KMC124

08KMC127

08KMC131

08KMC132

08XMC093

08XMC094

08XMC095

09AMC010

09CMC041

09EMC075

09EMC079

09EMC076

09GMC096

09GMC097

09GMC099

09JMC118

09JMC126

09KMC133

09KMC134

09XMC114

09XMC116

Product Description:
TYLENOL® ARTHRITIS CAPLET 100CT - (NOVEMBER 2009 RECALL)

NDC Code #
50580-112-10

UPC #300450838216
LOT #s

08BMC013

08BMC020

09BMC034

09CMC036

09CMC040

 

Product Description:
TYLENOL® EXTRA STRENGTH PM CAPLET 100+20CT

NDC Code #
50580-482-13

UPC #300450482136
LOT #s

ALA251

 

Product Description:
TYLENOL® EXTRA STRENGTH PM CAPLET 100CT

NDC Code #
50580-482-10

UPC #300450482105
LOT #s

AJA174

ALA250

Product Description:
TYLENOL® EXTRA STRENGTH PM CAPLET 150CT

NDC Code #
50580-482-15

UPC #300450482150
LOT #s

SEA188

 

TYLENOL® EXTRA STRENGTH PM CAPLET 225CT

NDC Code #
50580-482-35

UPC #300450482358
LOT #s

ABA415

ACA033
ACA440 ACA441
ADA179 ADA418
AEA073 AFA278
AFA319 AHA067
AJA181 ALA255
AMA053 AMA176
AMA349 APA010
APA216 SFA084
SHA044 SHA157
SHA230 SJA026
SLA050 SLA272
SMA081 SSA158

Product Description:
TYLENOL® EXTRA STRENGTH PM CAPLET 24+12CT

NDC Code #
50580-482-31

UPC #300450482310
LOT #s

AJA027

 

Product Description:
TYLENOL® EXTRA STRENGTH PM CAPLET 24CT

NDC Code #
50580-482-24

UPC #300450482242
LOT #s

AJA026

ABA021

ABA368

AJA025

ACA005

ADA259

Product Description:
TYLENOL® EXTRA STRENGTH PM CAPLET 50CT

NDC Code #
50580-482-50

UPC #300450482501
LOT #s

AFA005

AFA280
AFA289 AFA357

Product Description:
TYLENOL® EXTRA STRENGTH PM GELTAB 24CT

NDC Code #
50580-176-24

UPC #300450176240
LOT #s

ABA001

ABA370
AFA310 AHA083
AJA051  

Product Description:
TYLENOL® EXTRA STRENGTH PM GELTAB 50+20CT

NDC Code #
50580-176-70

UPC #300450176707
LOT #s

AJA098

 

Product Description:
TYLENOL® EXTRA STRENGTH PM GELTAB 50CT

NDC Code #
50580-176-50

UPC #300450176509
LOT #s

AFA177

AFA326

AFA100

 

Product Description:
TYLENOL® PM RAPID RELEASE GELCAP 20CT

NDC Code #
50580-244-20

UPC #300450244208
LOT #s

ABA002

ABA265
ADA281 AFA327
ACA004  

Product Description:
TYLENOL® PM RAPID RELEASE GELCAP 40CT

NDC Code #
50580-244-40

UPC #300450244406
LOT #s

ACA422

AEA077
AEA258 AFA059
AFA192 AHA172

Product Description:
TYLENOL® DAY & NIGHT VALUE PACK (TYLENOL® EXTRA STRENGTH 50CT + TYLENOL® PM 24CT)

NDC Code #
50580-527-10

UPC # 300450527103
LOT #s

AEC005

AFC005

ADC002

 

RECALL INFORMATION ON CERTAIN PRODUCT LOTS OF CHILDREN’S TYLENOL®

Product Description:
CHILDREN’S TYLENOL® BUBBLEGUM MELTAWAY 30 COUNT

NDC Code #
50580-519-30

UPC # 300450519306
LOT #s

AHA069

SPA022

ABA544

 

Product Description:
CHILDREN’S TYLENOL® GRAPE MELTAWAY 30 COUNT

NDC Code #
50580-518-30

UPC # 300450518309
LOT #s

AHA023

AHA057

Go to Tylenol.com for more information or click here to find a store near you that has the product you are looking for.


Only Certain Product LOTS are being Recalled as part of the July 8, 2010 and January 15, 2010 recalls of Over-the-Counter (OTC) products.

To find out if your MOTRIN® product has been recalled, please enter its LOT # here

If your MOTRIN® product LOT # is recalled, you will be taken to the product details on this page.

If the product lot # you enter is not part of the July 8, 2010 recall of Over-the-Counter (OTC) products, you will get a message letting you know. Click here for information on other recalls.

NOTE: Please be sure to enter both numeric and alphabetic characters correctly to find the exact LOT #. If you are unsure of whether a character is numeric (ex. the number 0) or alphabetic (ex. the letter O), please call our Consumer Care Center at 1-888-222-6036 and someone will help you verify.


Below you will find more details on specific products that are recalled. To find out if you have a product that is affected, please locate the NDC number and the lot number of the product you have. This information can be found on the box that the product was sold in and on the actual bottle itself. If you need help with finding this information, please call our Consumer Care Center at 1-888-222-6036.

Click here for information on other recalls.

Recall information on certain product lots of MOTRIN®

Product Description:
MOTRIN® IB TABLET 24 COUNT

NDC Code # 50580-109-02

UPC # 300450463029
LOT #s

ABA003

ADA258

AFA309

AJA055

Product Description:
MOTRIN® IB TABLET 50 COUNT

NDC Code # 50580-109-03

UPC # 300450463036
LOT #s

ABA004

ABA152

AFA228

AHA024

AJA007

AJA243

Product Description:
MOTRIN® IB TABLET 100 COUNT

NDC Code # 50580-109-04

UPC # 300450463043
LOT #s

AEA078

AEA261

AFA241

AFA060

Product Description:
MOTRIN® IB TABLET 100+25 COUNT

NDC Code # 50580-109-29

UPC # 300450463296
LOT #s

AFA017

AJA168

Product Description:
MOTRIN® IB TABLET 100+50 COUNT

NDC Code # 50580-109-75

UPC # 300450463753
LOT #s

ALA109

 

Product Description:
MOTRIN® IB CAPLET 24 COUNT

NDC Code # 50580-110-03

UPC # 300450481030
LOT #s

AAA435

ABA369

ADA174

AHA026

AJA006

ACA003

Product Description:
MOTRIN® IB CAPLET 24+6 COUNT

NDC Code # 50580-110-64

UPC # 300450481641
LOT #s

ADA246

 

Product Description:
MOTRIN® IB CAPLET 50 COUNT

NDC Code # 50580-110-02

UPC # 300450481023
LOT #s

ABA153

ABA541

ADA173

AHA025

Product Description:
MOTRIN® IB CAPLET BONUS PACK 50+25 COUNT

NDC Code # 50580-110-76

UPC # 300450481764
LOT #s

ACA002

 

Product Description:
MOTRIN® IB CAPLET 100 COUNT

NDC Code # 50580-110-01

UPC # 300450481016
LOT #s

ABA019

ACA469

ADA245

AEA260

AFA015

AJA049

AJA186

 

Product Description:
MOTRIN® IB CAPLET 100+25 COUNT

NDC Code # 50580-110-95

UPC # 300450481955
LOT #s

ADA287

AFA016

Product Description:
MOTRIN® IB CAPLET 100+50 COUNT

NDC Code # 50580-110-75

UPC # 300450481757
LOT #s

ABA538

AJA023

AJA120

 

Product Description:
MOTRIN® IB CAPLET 225 COUNT

NDC Code # 50580-110-62

UPC # 300450481627
LOT #s

24526

24544

24591

24604

24634

24687

24762

24794

24795

24818

24864

24905

24915

24935

24939

24977

25013

25044

25980

25996

26051

26085

26134

26192

26241

26335

26423

26455

26508

26533

Product Description:
MOTRIN® IB CAPLET 300 COUNT

NDC Code # 50580-110-37

UPC # 300450481375
LOT #s

ACA442

ACA759

ADA018

ADA419

AFA098

AFA112

AHA034

AHA068

ALA254

ALA359

AMA177

AMA350

APA217

SEA208

SFA184

SFA259

SHA107

SJA131

SLA049

SLA162

SMA013

SMA082

SSA157

 

Product Description:
JUNIOR STRENGTH MOTRIN® IB GRAPE CHEWABLE 24CT

NDC Code # 50580-909-24

UPC # 300450909244
LOT #s

ADM006

ADM052

AFM016

AFM350

AHM420

AJM346

ALM344

ALM399

AMM379

APM303

APM418

APM429

SLM084

Product Description:
JUNIOR STRENGTH MOTRIN® IB CAPLET 24CT

NDC Code # 50580-498-24

UPC # 300450498243
LOT #s

AJM322

APM348

Product Description:
JUNIOR STRENGTH MOTRIN® IB ORANGE CHEWABLE 24CT

NDC Code # 50580-207-24

UPC # 300450494245
LOT #s

ADM013

AFM024

AHM402

AJM345

ALM326

ALM456

AMM381

APM306

APM421

Go to Motrin.com for more information or click here to find a store near you that has the product you are looking for.


Only Certain Product LOTS are being Recalled as part of the January 15, 2010 recall of Over-the-Counter (OTC) products.

To find out if your SIMPLY SLEEP® product has been recalled, please enter its LOT # here

If your SIMPLY SLEEP® product LOT # is recalled, you will be taken to the product details on this page.

If the product lot # you enter is not part of the January 15, 2010 recall of Over-the-Counter (OTC) products, you will get a message letting you know. Click here for information on other recalls.

NOTE: Please be sure to enter both numeric and alphabetic characters correctly to find the exact LOT #. If you are unsure of whether a character is numeric (ex. the number 0) or alphabetic (ex. the letter O), please call our Consumer Care Center at 1-888-222-6036 and someone will help you verify.


Below you will find more details on specific products that are recalled. To find out if you have a product that is affected, please locate the NDC number and the lot number of the product you have. This information can be found on the box that the product was sold in and on the actual bottle itself. If you need help with finding the is information, please call our Consumer Care Center at 1-888-222-6036.

Recall information on certain product lots of SIMPLY SLEEP® MINI CAPLET

Product Description:
SIMPLY SLEEP® MINI CAPLET 100 COUNT

NDC Code # 50580-843-10

UPC # 300450843104
LOT #s

ADM015

ADM016

AFM014

AFM352

AJM319

AJM364

ALM387

AMM436

AMM438

 

Go to Tylenol.com for more information or click here to find a store near you that has the product you are looking for.


Only Certain Product LOTS are being Recalled as part of the January 15, 2010 recall of Over-the-Counter (OTC) products.

To find out if your ROLAIDS® product has been recalled, please enter its LOT # here

If your ROLAIDS® product LOT # is recalled, you will be taken to the product details on this page.

If the product lot # you enter is not part of the January 15, 2010 recall of Over-the-Counter (OTC) products, you will get a message letting you know. Click here for information on other recalls.

NOTE: Please be sure to enter both numeric and alphabetic characters correctly to find the exact LOT #. If you are unsure of whether a character is numeric (ex. the number 0) or alphabetic (ex. the letter O), please call our Consumer Care Center at 1-888-222-6036 and someone will help you verify.


Below you will find more details on specific products that are recalled. To find out if you have a product that is affected, please locate the NDC number and the lot number of the product you have. This information can be found on the box that the product was sold in and on the actual bottle itself. If you need help with finding this information, please call our Consumer Care Center at 1-888-222-6036.

Click here for information on other recalls.

Recall information on certain product lots of Rolaids® Antacid Tablets (150 and 100 count bottles)

Product Description:
ROLAIDS® EXTRA STRENGTH FRESHMINT 100 COUNT

NDC Code # 50580-746-01

UPC # 312547650212
LOT #s

AAA011

AAA083

AAA399

ABA397

ACA439

ADA086

ADA180

AEA197

AEA250

AFA053

AFA224

AFA293

AJA043

AJA114

ALA105

ALA159

ALA273

AMA178

APA054

SJA113

SJA114

SJA115

SJA116

SJA259

SLA149

SMA032

SMA222

SMA248

SPA024

SPA128

SPA161

SSA351

Product Description:
ROLAIDS® ORIGINAL PEPPERMINT TABLET 150 COUNT

NDC Code # 50580-772-15

UPC # 312547651158
LOT #s

AAA009

AAA202

AAA232

ABA141

ABA268

ABA416

ABA554

ACA567

ADA268

AEA072

AFA009

AFA171

AJA178

AMA024

AMA267

AMA268

APA041

SJA110

SJA111

SJA112

SJA148

SLA084

SLA217

SLA367

SLA370

SMA123

SMA124

SMA332

SPA129

SSA439

Product Description:
ROLAIDS® EXTRA STRENGTH FRUIT TABLET 100 COUNT

NDC Code # 50580-744-01

UPC # 312547650243
LOT #s

AAA086

ABA262

ACA256

ADA028

ADA082

AEA195

AFA234

AJA017

AJA018

AJA180

ALA026

AMA051

AMA208

APA152

SMA031

SMA099

SMA100

SMA101

SSA331

SSA332

Product Description:
ROLAIDS® ORIGINAL CHERRY TABLET 150 COUNT

NDC Code # 50580-773-15

UPC # 312547652421
LOT #s

ACA013

AEA057

AFA317

AJA016

AMA165

APA009

SLA087

SPA036

SSA334

SSA438

Product Description:
ROLAIDS® MULTI-SYMPTOM BERRY TABLET 100 COUNT

NDC Code # 50580-748-01

UPC # 312547654579
LOT #s

ABA009

ABA010

ABA011

ABA417

ABA620

ACA438

ALA256

APA042

ASA012

 

Product Description:
ROLAIDS® EXTRA STRENGTH TROPICAL PUNCH TABLET 100 COUNT

NDC Code # 50580-745-01

UPC # 312547654234
LOT #s

AAA359

SHA016

SHA017

SHA018

SJA204

SLA151

SSA175

 

Go to Rolaids.com for more information or click here to find a store near you that has the product you are looking for.


Only Certain Product LOTS are being Recalled as part of the January 15, 2010 recall of Over-the-Counter (OTC) products.

To find out if your ST. JOSEPH® product has been recalled, please enter its LOT # here

If your ST. JOSEPH® product LOT # is recalled, you will be taken to the product details on this page.

If the product lot # you enter is not part of the January 15, 2010 recall of Over-the-Counter (OTC) products, you will get a message letting you know. Click here for information on other recalls.

NOTE: Please be sure to enter both numeric and alphabetic characters correctly to find the exact LOT #. If you are unsure of whether a character is numeric (ex. the number 0) or alphabetic (ex. the letter O), please call our Consumer Care Center at 1-888-222-6036 and someone will help you verify.


Below you will find more details on specific products that are recalled. To find out if you have a product that is affected, please locate the NDC number and the lot number of the product you have. This information can be found on the box that the product was sold in and on the actual bottle itself. If you need help with finding the is information, please call our Consumer Care Center at 1-888-222-6036.

Click here for information on other recalls.

Recall information on certain product lots of ST. JOSEPH ASPIRIN.

Product Description:
ST. JOSEPH® ASPIRIN CHEWABLE ORANGE TABLET 36 COUNT

NDC Code # 50580-173-36

UPC # 300450173362
LOT #s

AHM440

AMM325

APM430

 

Product Description:
ST. JOSEPH® ASPIRIN CHEWABLE ORANGE TABLET 3x36 COUNT

NDC Code # 50580-173-08

UPC # 300450173089
LOT #s

AFM360

AHM423

ALM346

AMM434

Product Description:
ST. JOSEPH® ASPIRIN ENTERIC COATED TABLET 36 COUNT

NDC Code # 50580-126-36

UPC # 300450126368
LOT #s

AFM026

AHM327

AHM432

AJM321

ALM327

AMM324

APM349

APM420

Product Description:
ST. JOSEPH® ASPIRIN ENTERIC COATED TABLET 100 COUNT

NDC Code # 50580-126-10

UPC # 300450126108
LOT #s

AEM050

AHM374

AJM320

AJM402

ALM341

AMM365

AMM366

AMM367

APM350

APM351

Product Description:
ST. JOSEPH® ASPIRIN ENTERIC COATED TABLET 180 COUNT

NDC Code # 50580-126-18

UPC # 300450126184
LOT #s

AMM323

AMM433

APM304

 

Product Description:
ST. JOSEPH® ASPIRIN ENTERIC COATED TABLET 300 COUNT

NDC Code # 50580-126-03

UPC # 300450126030
LOT #s

AHM368

ALM377

ALM378

AMM354

APM427

 

Go to stjosephaspirin.com for more information or click here to find a store near you that has the product you are looking for.

Only Certain Product LOTS are being Recalled as part of the January 15, 2010 recall of Over-the-Counter (OTC) products.

To find out if your ST. JOSEPH® product has been recalled, please enter its LOT # here

If your ST. JOSEPH® product LOT # is recalled, you will be taken to the product details on this page.

If the product lot # you enter is not part of the January 15, 2010 recall of Over-the-Counter (OTC) products, you will get a message letting you know. Click here for information on other recalls.

NOTE: Please be sure to enter both numeric and alphabetic characters correctly to find the exact LOT #. If you are unsure of whether a character is numeric (ex. the number 0) or alphabetic (ex. the letter O), please call our Consumer Care Center at 1-888-222-6036 and someone will help you verify.


Below you will find more details on specific products that are recalled. To find out if you have a product that is affected, please locate the NDC number and the lot number of the product you have. This information can be found on the box that the product was sold in and on the actual bottle itself. If you need help with finding the is information, please call our Consumer Care Center at 1-888-222-6036.

Click here for information on other recalls.

Recall information on certain product lots of ST. JOSEPH ASPIRIN.

Product Description:
ST. JOSEPH® ASPIRIN CHEWABLE ORANGE TABLET 36 COUNT

NDC Code # 50580-173-36

UPC # 300450173362
LOT #s

AHM440

AMM325

APM430

 

Product Description:
ST. JOSEPH® ASPIRIN CHEWABLE ORANGE TABLET 3x36 COUNT

NDC Code # 50580-173-08

UPC # 300450173089
LOT #s

AFM360

AHM423

ALM346

AMM434

Product Description:
ST. JOSEPH® ASPIRIN ENTERIC COATED TABLET 36 COUNT

NDC Code # 50580-126-36

UPC # 300450126368
LOT #s

AFM026

AHM327

AHM432

AJM321

ALM327

AMM324

APM349

APM420

Product Description:
ST. JOSEPH® ASPIRIN ENTERIC COATED TABLET 100 COUNT

NDC Code # 50580-126-10

UPC # 300450126108
LOT #s

AEM050

AHM374

AJM320

AJM402

ALM341

AMM365

AMM366

AMM367

APM350

APM351

Product Description:
ST. JOSEPH® ASPIRIN ENTERIC COATED TABLET 180 COUNT

NDC Code # 50580-126-18

UPC # 300450126184
LOT #s

AMM323

AMM433

APM304

 

Product Description:
ST. JOSEPH® ASPIRIN ENTERIC COATED TABLET 300 COUNT

NDC Code # 50580-126-03

UPC # 300450126030
LOT #s

AHM368

ALM377

ALM378

AMM354

APM427

 

Go to stjosephaspirin.com for more information or click here to find a store near you that has the product you are looking for.

  Call Us TTY 800-722-1322 888-222-6036   Click here to email us.   Click here to request a refund or product coupon on certain recalls.