Acetaminophen by Meijer ACETAMINOPHEN tablet

Acetaminophen by

Drug Labeling and Warnings

Acetaminophen by is a Otc medication manufactured, distributed, or labeled by Meijer. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient (in each coated tablet)

Acetaminophen USP, 500mg

Purpose

Pain reliever/fever reducer

Uses

 temporarily relieves minor aches and pains due to:

 the common cold  headache
 backache  minor pain of arthritis
 toothache  muscular aches
 premenstrual and menstrual cramps

 temporarily reduces fever

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

Ask a doctor before use if you have

liver disease

Ask a doctor or pharmacist before use if you are

taking the blood thinning drug warfarin

Stop use and ask a doctor if

 pain gets worse or lasts more than 10 days
 fever gets worse or lasts more than 3 days
 new symptoms occur
 redness or swelling is present

These could be signs of a serious condition

If pregnant or breast-feeding,

​ask a health professional before use

Keep out of reach of children

Keep out of reach of children

Overdose warning:

In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222) Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

 do not take more than directed (see overdose warning)

adults and children 12  take 2 tablets every 6 hours while symptoms last
years and over  do not take more than 6 tablets in 24 hours, unless directed by a doctor
 do not use for more than 10 days unless directed by a doctor

children under  ask a doctor
12 years

Other information

 store at 20°-25°C (68°-77°F). See USP Controlled Room Temperature.
 see bottom of the label for lot number and expiration date

Inactive ingredients

FD&C red no. 40, FD&C yellow no. 6, lecithin, polyethylene glycol, polyvinyl alcohol, povidone k-30, pregelatinized starch, stearic acid, sucralose, talc, titanium dioxide

Questions or comments?

call 1-877-770-3183 Mon-Fri 8:00 AM EST to 5:00 PM PST

PDP

INGREDIENTS AND APPEARANCE

ACETAMINOPHEN 
acetaminophen tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79481-5380
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
POVIDONE K30 (UNII: U725QWY32X)
STARCH, CORN (UNII: O8232NY3SJ)
FD&C RED NO. 40 (UNII: WZB9127XOA)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TALC (UNII: 7SEV7J4R1U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
STEARIC ACID (UNII: 4ELV7Z65AP)
SUCRALOSE (UNII: 96K6UQ3ZD4)

Product Characteristics
Color	red	Score	no score
Shape	ROUND	Size	11mm
Flavor		Imprint Code	L;1
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79481-5380-2	225 in 1 BOTTLE; Type 0: Not a Combination Product	09/09/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M013	09/09/2024

Labeler - Meijer (006959555)