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

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Equate Pain Reliever Acetaminophen for Adults 250 mg

Active ingredient (in each chewable bar)

Acetaminophen 250mg

Purpose

Pain reliever/fever reducer

Uses

Warnings

Liver warning: this product contains acetaminophen. Severe liver damage may occur if you take

Allergy alert:

acetaminophen may cause severe skin reactions. Symptoms may include:

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

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

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

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.

Equate Pain Reliever Acetaminophen for Adults 250 mg

EQUATE PAIN RELIEVER ACETAMINOPHEN FOR ADULTS 250 MG 
acetaminophen bar, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-238
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN250 mg
Inactive Ingredients
Ingredient NameStrength
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
Colorpurple (Dark Purple) Scoreno score
ShapeRECTANGLESize25mm
FlavorBLUEBERRY (Cool Blueberry) Imprint Code O
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79903-238-4040 in 1 BOTTLE; Type 0: Not a Combination Product06/01/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01306/01/2024
Labeler - Walmart Inc (051957769)
Establishment
NameAddressID/FEIBusiness Operations
USpharma Ltd080664601manufacture(79903-238)

Revised: 3/2024
Document Id: 143326a3-9a61-4dc6-e063-6294a90af9c4
Set id: 08a18481-f029-f01f-e063-6294a90aac65
Version: 2
Effective Time: 20240321
 
Walmart Inc