Label: PAIN RELIEF EXTRA STRENGTH- acetaminophen tablet, film coated
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Contains inactivated NDC Code(s)
NDC Code(s): 59779-751-03, 59779-751-29, 59779-751-96 - Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated August 21, 2019
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each caplet)
- Purpose
- Uses
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Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take
- more than 4,000 mg of acetaminophen in 24 hours
- with other drugs containing acetaminophen
- 3 or more alcoholic drinks every day while using this product
Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
- rash
- skin reddening
- blisters
If a skin reaction occurs, stop use and seek medical help right away.
Do not use
- with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
- if you are allergic to acetaminophen or any of the inactives ingredients in this product.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
♥︎CVS
Health™
Compare to the active ingredient in Extra Strength Tylenol®*
Caplets
TAMPER EVIDENT: Use Only if This Blister is Intact
NDC 59779-751-03
EXTRA STRENGTH
Pain Relief
ACETAMINOPHEN, 500 mg
Pain reliever / Fever reducerAspirin free
10 CAPLETS Actual Size
Travel Pack
†This product is not manufactured or distributed by Johnson & Johnson Corporation, owner of the registered trademark Extra Strength Tylenol®.
50844 REV0617A17503Distributed by:CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
© 2017 CVS/pharmacy
CVS.com® 1-800-SHOP-CVS
V-13566CVS® Quality
Money Back GuaranteeCVS Health 44-175
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INGREDIENTS AND APPEARANCE
PAIN RELIEF EXTRA STRENGTH
acetaminophen tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-751 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg Inactive Ingredients Ingredient Name Strength HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) STEARIC ACID (UNII: 4ELV7Z65AP) CASTOR OIL (UNII: D5340Y2I9G) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color WHITE Score no score Shape OVAL Size 17mm Flavor Imprint Code 44;175 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-751-03 1 in 1 PACKAGE 04/02/1993 1 10 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:59779-751-96 2 in 1 PACKAGE 04/02/1993 2 10 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:59779-751-29 1 in 1 CARTON 04/02/1993 10/20/2015 3 150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part343 04/02/1993 Labeler - CVS Pharmacy (062312574) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 PACK(59779-751) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 MANUFACTURE(59779-751) , PACK(59779-751) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 PACK(59779-751) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 PACK(59779-751)