EQUATE PAIN RELIEVER ACETAMINOPHEN FOR ADULTS 250 MG- acetaminophen bar, chewable

Equate Pain Reliever Acetaminophen for Adults 250 mg by

Drug Labeling and Warnings

Equate Pain Reliever Acetaminophen for Adults 250 mg by is a Otc medication manufactured, distributed, or labeled by Walmart Inc, USpharma Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each chewable bar)

Acetaminophen 250mg

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 4,000mg of acetaminophen in 24 hours, which is the maximum daily amount
• 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
• a sodium-restricted diet

Ask a doctor or pharmacist before use if you aretaking 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.

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 give more than directed (see overdose warning)

• Age (yrs.): Dose (chewable bar)
• Adults and children 12 years and over:
  • take 4 chewable bars every 6 hours while symptoms last
  • do not take more than 12 chewable bars 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

• each chewable bar contains: potassium 5mg, sodium 17mg.
• Store in a cool dry place between 20-25°C (68-77°F).
• Child Resistant Container;do not use if printed seal under cap is broken or missing.

Inactive ingredients:

ammonium glycyrrhizate, D & C red # 33, FD & C blue # 1, flavors, geleol mono and diglycerides, glucose syrup, hydroxypropyl betadex, maltitol solution, maltodextrin, menthol, neotame, polyethylene glycol 400, povidone, propylene glycol, purified water, seaweed extract (carrageenan), sodium chloride, starch, sucralose, sucrose, trisodium citrate dihydrate.

Questions or comments?

Call  1-888-287-1915

SPL UNCLASSIFIED SECTION

U.S. Patent 11,273,123

Principal Display Panel - Equate Pain Reliever Acetaminophen for Adults 250 mg-Cool Blueberry Flavor

NDC: 79903-238-40

equate™

Compare to Tylenol ®active ingredient**

Pain Reliever Acetaminophen for Adults 250 mg

Pain Reliever/Fever Reducer

Contains No Aspirin

Soft Chew Bars

Cool Bluberry Flavor

250 mg EACH     40 CHEWABLE BARS

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

INGREDIENTS AND APPEARANCE

EQUATE PAIN RELIEVER ACETAMINOPHEN FOR ADULTS 250 MG 
acetaminophen bar, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-238
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	250 mg

Inactive Ingredients
Ingredient Name	Strength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POVIDONE K30 (UNII: U725QWY32X)
CORN SYRUP (UNII: 9G5L16BK6N)
HYDROXYPROPYL BETADEX (UNII: 1I96OHX6EK)
NEOTAME (UNII: VJ597D52EX)
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
GLYCERYL MONO AND DIPALMITOSTEARATE (UNII: KC98RO82HJ)
SUCRALOSE (UNII: 96K6UQ3ZD4)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CARRAGEENAN (UNII: 5C69YCD2YJ)
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
SUCROSE (UNII: C151H8M554)
MALTITOL (UNII: D65DG142WK)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
LEVOMENTHOL (UNII: BZ1R15MTK7)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
WATER (UNII: 059QF0KO0R)
STARCH, CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	purple (Dark Purple)	Score	no score
Shape	RECTANGLE	Size	25mm
Flavor	BLUEBERRY (Cool Blueberry)	Imprint Code	O
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-238-40	40 in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M013	06/01/2024

Labeler - Walmart Inc (051957769)

Establishment
Name	Address	ID/FEI	Business Operations
USpharma Ltd		080664601	manufacture(79903-238)