NDC | 37012-484-71, 37012-484-78, 37012-484-85, 37012-484-90 |
Set ID | 51cb7067-769f-4ea0-94f4-610db816458b |
Category | HUMAN OTC DRUG LABEL |
Packager | Shopko Stores Operating Co., LLC |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART343 |
- 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:
- •
- 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 have ever had an allergic reaction to this product or any of its ingredients
-
Directions
- •
- do not take more than directed (see overdose warning)
adults and children 12 years and over
- •
- take 2 caplets every 6 hours while symptoms last
- •
- do not take more than 6 caplets in 24 hours, unless directed by a doctor
- •
- do not use for more than 10 days unless directed by a doctor
children under 12 years
ask a doctor
- Other information
- Inactive ingredients
- Questions or comments?
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
PAIN RELIEF
acetaminophen tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37012-484 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 CARNAUBA WAX (UNII: R12CBM0EIZ) STARCH, CORN (UNII: O8232NY3SJ) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) STEARIC ACID (UNII: 4ELV7Z65AP) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) Product Characteristics Color WHITE Score no score Shape OVAL Size 16mm Flavor Imprint Code L484 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37012-484-71 1 in 1 CARTON 08/08/2013 1 50 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:37012-484-85 1 in 1 CARTON 08/08/2013 2 250 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:37012-484-90 500 in 1 BOTTLE; Type 0: Not a Combination Product 08/08/2013 4 NDC:37012-484-78 1 in 1 CARTON 08/08/2013 4 100 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 08/08/2013 Labeler - Shopko Stores Operating Co., LLC (023252638)