- Active ingredient (in each gelcap)
- 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 inactive ingredients in this product
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
CORE VALUES™
Compare to active ingredient in Extra Strength Tylenol® Rapid Release†
Extra Strength
Pain Reliever
Acetaminophen 500 mg
Pain Reliever/Fever Reducer
Contains No Aspirin • Rapid ReleaseActual Size
24 Gelcaps
†This product is not manufactured or distributed by Johnson & Johnson Corporation, owner of the registered trademark Extra Strength Tylenol® Rapid Release.
50844 ORG041751908Distributed by:
Liberty Procurement Co. Inc.,
650 Liberty Ave., Union, NJ 07083 U.S.ASatisfaction Guaranteed Or Your Money Back
Visit us at www.facevalues.comCore Values 44-519
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INGREDIENTS AND APPEARANCE
PAIN RELIEVER EXTRA STRENGTH
acetaminophen tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63940-519 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 CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) GELATIN (UNII: 2G86QN327L) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) FERROSOFERRIC OXIDE (UNII: XM0M87F357) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE (UNII: FZ989GH94E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SHELLAC (UNII: 46N107B71O) STEARIC ACID (UNII: 4ELV7Z65AP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH) STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color blue, red Score no score Shape OVAL Size 19mm Flavor Imprint Code L;5 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63940-519-19 1 in 1 PACKAGE 05/10/2004 05/07/2021 1 8 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:63940-519-08 1 in 1 CARTON 05/10/2004 2 24 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:63940-519-29 150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/10/2004 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part343 05/10/2004 Labeler - Harmon Store Inc. (804085293) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(63940-519) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(63940-519) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(63940-519) , pack(63940-519) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 pack(63940-519)