Label: CHILDRENS ALLERGY RELIEF- diphenhydramine hcl solution

  • NDC Code(s): 79903-411-04, 79903-411-08
  • Packager: WALMART INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 22, 2026

If you are a consumer or patient please visit this version.

View All Sections
  • Active ingredient (in each 5 mL)

    Diphenhydramine HCl 12.5 mg

  • Purpose

    Antihistamine

  • Uses

    • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
      • runny nose
      • sneezing
      • itchy, watery eyes
      • itching of the nose or throat
  • Warnings

    Do not use

    • to make a child sleepy
    • with any other product containing diphenhydramine, even one used on skin

    Ask a doctor before use if the child has

    • a breathing problem such as chronic bronchitis
    • glaucoma

    Ask a doctor or pharmacist before use if the child is

    taking sedatives or tranquilizers.

    When using this product

    • marked drowsiness may occur
    • sedatives and tranquilizers may increase drowsiness
    • excitability may occur, especially in children

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions

    • do not take more than directed
    • do not take more than 6 doses in 24 hours
    • mL = milliliter
    • only use the dose cup provided
    • find right dose on chart below
    • take every 4 to 6 hours, or as directed by a doctor
    Age (yr)Dose (mL)
    children under 2 yearsdo not use
    children 2 to 5 yearsdo not use unless directed by a doctor
    children 6 to 11 years5 mL to 10 mL
  • Other information

    • each 5 mL contains: sodium 4 mg
    • store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
    • see end flap for expiration date and lot number
  • Inactive ingredients

    anhydrous citric acid, flavor, glycerin, propylene glycol, purified water, sodium benzoate, sodium chloride, sodium citrate dihydrate, sucralose, xanthan gum

  • Questions or comments?

    1-888-287-1915

  • Principal display panel

    equate™

    NDC 79903-411-04

    Compare
    to Children’s
    Benadryl®
    Allergy active
    ingredient*

    children's 
    ALLERGY RELIEF
    Diphenhydramine HCl,
    12.5 mg per 5 mL
    Oral Solution
    Antihistamine

    DYE-FREE
    ALCOHOL-FREE
    SUGAR-FREE
    6-11 YEARS

    Relieves:
    • Runny nose
    • Sneezing
    • Itchy, watery eyes
    • Itchy throat or nose

    Clear
    Cherry Flavored

    4 FL OZ (118 mL)

    Dosage Cup
    Included

    TAMPER EVIDENT: DO NOT USE IF PRINTED
    NECKWRAP IS BROKEN OR MISSING 

    Satisfaction Guaranteed
    For more information call
    1-888-287-1915
    or visit Walmart.com./help

    DISTRIBUTED BY: Walmart Inc.,
    Bentoville, AR 72716
    PRODUCT OF CHINA
    *This product is not manufactured or
    distributed by Kenvue Inc., owner of the
    registered trademark Children's Benadryl®
    Allergy. 50844 ORG082401736 

    Equate 44-017

    Equate 44-017

  • INGREDIENTS AND APPEARANCE
    CHILDRENS ALLERGY RELIEF 
    diphenhydramine hcl solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-411
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE12.5 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorCHERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-411-041 in 1 CARTON05/26/2026
    1118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:79903-411-081 in 1 CARTON05/26/2026
    2237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01205/26/2026
    Labeler - WALMART INC. (051957769)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.967626305manufacture(79903-411) , pack(79903-411)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!