Label: ALLERGY RELIEF- diphenhydramine hcl capsule, liquid filled

  • NDC Code(s): 79481-0880-1
  • Packager: Meijer Distribution Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 26, 2024

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

  • Active ingredient (in each capsule)

    Diphenhydramine HCl 25 mg

  • Purpose

    Antihistamine

  • Uses

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

  • Warnings

    ■ May cause excitability especially in children.
    ■ May cause marked drowsiness; alcohol, sedatives, and tranquilizers may increase the drowsiness effect.

  • Do not use

    ■ Do not use for children under 6 years of age ■ with any other product containing diphenhydramine, even one used on skin.

  • Ask a doctor before use if you have

    ■ glaucoma ■ a breathing problem such as emphysema or chronic bronchitis ■ difficulty in urination due to enlargement of the prostate gland

  • Ask a doctor or pharmacist before use

    if you are taking sedatives or tranquilizers.

  • When using this product

    ■ avoid alcoholic beverages ■ be careful when driving a motor vehicle or operating machinery

  • Stop use and ask a doctor if

    sleeplessness persists continuously for more than 2 weeks

  • If pregnant or breast-feeding,

    ask a health professional before use.

  • Keep out of reach of children.

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

  • Directions

    ■ Do not use for children under 6 years of age ■ do not take more than 6 doses in 24 hours

    adults and children 12 years and over1 to 2 capsules
    children 6 to under 12 years1 capsule
    children under 6 yearsdo not use this product for children under 6 years of age

  • Other information

    ■ store at 20°C to 25°C (68°F to 77°F)
    ■ avoid high humidity and excessive heat above 40°C (104°F).
    ■ protect from light

  • Inactive ingredients

    gelatin, glycerin, polyethylene glycol 400, propylene glycol, purified water, sorbitol sorbitan solution

  • Questions or comments?

    call toll-free 1-888-235-2466 (Mon - Fri 9AM - 5PM EST)

  • SPL UNCLASSIFIED SECTION

    THIS PRODUCT IS PACKAGED IN A TAMPER EVIDENT PACKAGE.
    USE ONLY IF BLISTERS ARE INTACT.

    KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.

    †This product is not manufactured or distributed by Kenvue, Inc. and Catalent Solutions, Inc., respective owners of the
    registered trademarks Benadryl® and Liqui-gels®.

    DIST. MEIJER DISTRIBUTION, INC.
    GRAND RAPIDS, MI 49544
    www.meijer.com

    Made in India
    Mfg. Lic. No.: TN00002123

    R0924
    L0000910

  • 24's count

    NDC 79481-0880-1

    Compare to the active ingredient in Benadryl ® Allergy LIQUI-GELS ®†

    meijer

    DYE-FREE

    Allergy Refief

    • SNEEZING • RUNNY NOSE

    • ITCHY, WATERY EYES • ITCHY THROAT OR NOSE

    DIPHENHYDRAMINE HCl CAPSULES
    USP, 25 mg

    ANTIHISTAMINE

    24 softgels*

    *liquid-filled capsules

    image001

  • INGREDIENTS AND APPEARANCE
    ALLERGY RELIEF 
    diphenhydramine hcl capsule, liquid filled
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79481-0880
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
    Inactive Ingredients
    Ingredient NameStrength
    SORBITAN (UNII: 6O92ICV9RU)  
    GELATIN (UNII: 2G86QN327L)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    Colorwhite (Clear) Scoreno score
    ShapeCAPSULESize17mm
    FlavorImprint Code DF25
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79481-0880-12 in 1 CARTON11/26/2024
    112 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01211/26/2024
    Labeler - Meijer Distribution Inc (006959555)
    Registrant - Bionpharma Inc. (079637826)
    Establishment
    NameAddressID/FEIBusiness Operations
    SOFTGEL HEALTHCARE PRIVATE LIMITED675584180manufacture(79481-0880)