Label: AFTER BITE PLUS- diphenhydramine hcl gel

  • NDC Code(s): 44224-0176-0, 44224-0176-1
  • Packager: Tender Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 26, 2023

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  • Active Ingredient

    Diphenhydramine HCl 2%

  • Purpose

    Topical Analgesic

  • Uses

    For the temporary relief of pain and itching associated with

    • insect bites
    • minor burns
    • sunburn
    • minor skin irritations
    • minor cuts
    • rashes due to poison ivy, poison oak, and poison sumac
  • Warnings

    For external use only

  • Do not use

    Do not use

    • on large areas of the body
    • with any other product containing diphenhydramine, even one taken by mouth
  • Ask a doctor before use

    Ask a doctor before use

    • on chicken pox
    • on measles
  • When using

    When using this product avoid contact with eyes.

  • Stop use and ask a doctor if

    Stop use and ask a doctor if

    • condition worsens
    • if symptoms persist for more than 7 days or clear up and occur again within a few days
  • Keep out of reach of children

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Directions

    • do not use more than directed
    • adults and children over 2 years of age and older: apply to affected area not more than 3 to 4 times daily
    • children under 2 years of age: ask a doctor
  • Inactive Ingredients

    Aloe Vera, Citric Acid, Ethyl Alcohol, Glycerin, Methocel, Methylparaben, Oat Beta Glucan, Propylparaben, Purified Water, Sodium Hydroxide, Tea Tree Oil, Vitamin E

  • Package Labeling

    Plus

  • INGREDIENTS AND APPEARANCE
    AFTER BITE PLUS 
    diphenhydramine hcl gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44224-0176
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    ALCOHOL (UNII: 3K9958V90M)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    METHYLCELLULOSE (100 CPS) (UNII: 4GFU244C4J)  
    OAT (UNII: Z6J799EAJK)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44224-0176-11 in 1 BOX03/01/201809/30/2020
    120 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:44224-0176-020 g in 1 TUBE; Type 0: Not a Combination Product03/01/201809/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/01/201812/31/2024
    Labeler - Tender Corporation (064437304)
    Registrant - Tender Corporation (064437304)
    Establishment
    NameAddressID/FEIBusiness Operations
    Tender Corporation064437304manufacture(44224-0176)
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