- Active ingredient (in each tablet)
- Purpose
- Uses
-
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if
- adult takes more than 4,000 mg of acetaminophen in 24 hours
- child takes more than 5 doses in 24 hours
- taken with other drugs containing acetaminophen
- adult has 3 or more alcoholic drinks every day while using this product
Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
- skin reddening
- blisters
- rash
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
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Directions
- do not take more than directed
adults and children 12 years and over ■ take 2 tablets every 4 to 6 hours while symptoms last
■ do not take more than 10 tablets in 24 hours
■ do not take for more than 10 days unless directed by a doctorchildren 6-11 years ■ take 1 tablet every 4 to 6 hours while symptoms last
■ do not take more than 5 tablets in 24 hours
■ do not take for more than 5 days unless directed by a doctorchildren under 6 years ask a doctor - Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
fred's
PharmacyNDC 55315-105-12
Compare to the active ingredient in:
Regular Strength Tylenol®*
Regular Strength
PAIN RELIEVER
Acetaminophen, 325 mg
Pain Reliever/Fever Reducer100 TABLETS
Actual
SizeTAMPER EVIDENT: DO NOT USE IF IMPRINTED
SAFETY SEAL UNDER CAP IS BROKEN OR MISSING*This product is not manufactured or distributed by
Johnson & Johnson Corporation, owner of the registered
trademark Regular Strength Tylenol®.
50844 REV0417A10412DISTRIBUTED BY: fred's, Inc.
4300 NEW GETWELL RD, MEMPHIS, TN 38118
www.fredsinc.com100% satisfaction guaranteed
Freds Pharmacy 44-104
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INGREDIENTS AND APPEARANCE
PAIN RELIEVER REGULAR STRENGTH
acetaminophen tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55315-105 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) STEARIC ACID (UNII: 4ELV7Z65AP) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) Product Characteristics Color WHITE Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code 44;104 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55315-105-12 1 in 1 CARTON 07/13/1990 04/08/2022 1 100 in 1 BOTTLE; 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 07/13/1990 04/08/2022 Labeler - FRED'S, INC. (005866116) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 PACK(55315-105) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 MANUFACTURE(55315-105) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 PACK(55315-105) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 PACK(55315-105)