Label: AXIV ALLERGY- diphenhydramine hydrochloride capsule, liquid filled

  • NDC Code(s): 82706-019-01, 82706-019-02
  • Packager: VIVUNT LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 8, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active Ingredient (in each softgel)Purpose
    Diphenhydramine HCl 25 mgAntihistamine

  • 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
    • temporarily relieves these symptoms due to the common cold:
    • runny nose
    • sneezing
  • 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 you have

    • a breathing problem such as emphysema or chronic bronchitis
    • glaucoma
    • trouble urinating due to an enlarged prostate gland

    Ask a doctor or pharmacist before use if you are

    taking sedatives or tranquilizers

    When using this product

    • marked drowsiness may occur
    • avoid alcoholic drinks
    • alcohol, sedatives, and tranquilizers may increase drowsiness
    • be careful when driving a motor vehicle or operating machinery
    • excitability may occur, especially in children

    Keep out of reach of children

    Keep out of reach of children.

    If pregnant or breast-feeding

    ask a health professional before use.

    Overdose Warning

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

  • Directions

    • Take every 4 to 6 hours, or as directed by a doctor
    • Do not take more than 12 Softgels in 24 hours for Adults and children 12 years and over. Do not take more than 6 Softgels for children 6 to under 12 years of age in 24 hours.

    adults and children 12 years and over1 or 2 Softgels
    children 6 to under 12 years1 Softgel
    children under 6 yearsdo not use
  • Other information

    • Store at 20° - 25 °C (68 °- 77 °F)
    • Read all product information before using
    • Tamper Evident: Do not use if the foil printed on the blister is torn or ripped.
    • Tamper Evident: Do not use if carton or pouch is open
  • Inactive ingredients

    Gelatin, Glycerin, Methylparaben, Polyethylene Glycol 400, Propylparaben, Purified Water, Sorbitol, Titanium Dioxide

  • PRINCIPAL DISPLAY PANEL 24

    Compare to Benadryl® Allergy Liqui-Gels®

    active ingredients*

    NDC 82706-019-01

    AXIV Antihistamine

    • Runny Nose
    • Sneezing
    • Itchy, Watery Eyes
    • Itchy Throat

    DYE-FREE

    Diphenhydramine HCl

    24 SOFTGELS** **Liquid-filled capsules

    AXIVALLER1

  • PRINCIPAL DISPLAY PANEL 6

    Compare to Benadryl® Allergy Liqui-Gels®

    active ingredients*

    NDC 82706-019-02

    AXIV Antihistamine

    Runny Nose
    Sneezing
    Itchy, Watery Eyes
    Itchy Throat

    DYE-FREE

    Diphenhydramine HCl

    6 SOFTGELS** **Liquid-filled capsules

    AXIVALLER1C

  • INGREDIENTS AND APPEARANCE
    AXIV ALLERGY 
    diphenhydramine hydrochloride capsule, liquid filled
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82706-019
    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
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    GELATIN (UNII: 2G86QN327L)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SORBITOL (UNII: 506T60A25R)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Colorwhite (Transparent) Scoreno score
    ShapeOVALSize22mm
    FlavorImprint Code AXIV
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82706-019-012 in 1 CARTON03/08/2024
    112 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:82706-019-023 in 1 CARTON03/08/2024
    22 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01203/08/2024
    Labeler - VIVUNT LLC (045829437)
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