Label: ACETAMINOPHEN REGULAR STRENGTH- acetaminophen tablet, coated
- NDC Code(s): 46122-430-78
- Packager: Amerisource Bergen
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 11, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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:
- 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
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
NDC 46122-430-78
Good
Neighbor
Pharmacy®Compare to
Regular Strength Tylenol®
active ingredient*REGULAR STRENGTH
Acetaminophen
325 mgPain Reliever / Fever Reducer
100
Gelcaps
325 mg EachActual Size
TAMPER EVIDENT: DO
NOT USE IF IMPRINTED
SAFETY SEAL UNDER
CAP IS BROKEN OR
MISSINGDistributed By
AmerisourceBergen
1 West First Avenue
Conshohocken, PA 19428
Questions or Concerns?
www.mygnp.comGood Neighbor Pharmacy Brand Products
Satisfaction Guaranteed*This product is not
manufactured or distributed
by Johnson & Johnson
Corporation, owner of the
registered trademark Regular
Strength Tylenol®.
50844 REV0421B67812Good Neighbor 44-678
-
INGREDIENTS AND APPEARANCE
ACETAMINOPHEN REGULAR STRENGTH
acetaminophen tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:46122-430 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) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) GELATIN, UNSPECIFIED (UNII: 2G86QN327L) HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SHELLAC (UNII: 46N107B71O) STEARIC ACID (UNII: 4ELV7Z65AP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color red, white Score no score Shape OVAL Size 16mm Flavor Imprint Code LB Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:46122-430-78 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/24/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 07/24/2015 Labeler - Amerisource Bergen (007914906) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 manufacture(46122-430) , pack(46122-430) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(46122-430) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(46122-430) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(46122-430)