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 16mg.
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, FD & C yellow #6, 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

U.S. Patent 11,273,123

Principal Display Panel - Equate Pain Reliever Acetaminophen for Adults 250 mg-Orange Vanilla Flavor

NDC 79903-247-40

equate™

Compare to Tylenol ®active ingredient**

Pain Reliever Acetaminophen for Adults 250 mg

Pain Reliever/Fever Reducer

Contains No Aspirin

Soft Chew Bars

Orange Vanilla Flavor

250 mg EACH 40 CHEWABLE BARS

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

Equate Pain Reliever Acetaminophen for Adults 250 mg

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:79903-247
Route of Administration	ORAL

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

Ingredient Name	Strength
Inactive Ingredients
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)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
WATER (UNII: 059QF0KO0R)
STARCH, CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	orange	Score	no score
Shape	RECTANGLE	Size	25mm
Flavor	ORANGE (Orange Vanilla Flavor)	Imprint Code	O
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:79903-247-40	40 in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2024

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

Labeler - Walmart Inc (051957769)

Name	Address	ID/FEI	Business Operations
Establishment
USpharma Ltd		080664601	manufacture(79903-247)