- Active ingredient (in each caplet)
- Purpose
- Uses
-
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?
-
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
-
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)