Label: AFTER BITE ADVANCED- sodium bicarbonate liquid

  • NDC Code(s): 44224-1103-0, 44224-1103-2, 44224-1103-3
  • Packager: Tender Corporation d/b/a Adventure Ready Brands
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2025

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  • Active Ingredient / Purpose

    Sodium Bicarbonate (Baking Soda) 5% Skin Protectant

  • Uses

    Temproarily protects and helps relieve minor skin irritation and itching due to insect bite poison ivy, oak sumac

  • Warnings

    For external use only.

    if in eyes

    flush with water for 15 minutes call a doctor

  • When using this product

    do not get into eyes, do not bandage or cover until dry

  • Stop use and ask a doctor if

    condition worsens , symptoms last more than 7 days or clear up and oiccur again within a few days

  • Keep out of reach of children

    if swollowed, get medical help or contact poisin control center right away.

  • Directions

    Adults and children 2 years and older apply to the affected area of the skin as needed or as directed by a doctor

    Children under 2 years as a doctor

  • Inactive Ingredients

    Ammonia, glycerin, purified water

  • Purpose

    Skin Protectant

  • Box artwork

    Front of package Primary Packaging

  • Primary label

    Primary PackagingLabel on actual product

  • 3 Vial Box

    Secondary Packaging

  • INGREDIENTS AND APPEARANCE
    AFTER BITE ADVANCED 
    sodium bicarbonate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44224-1103
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20) SODIUM BICARBONATE0.7 g  in 14 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.14 g  in 14 g
    AMMONIA (UNII: 5138Q19F1X) 0.778 g  in 14 g
    WATER (UNII: 059QF0KO0R) 12.376 g  in 14 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44224-1103-21 in 1 BOX06/17/2025
    1NDC:44224-1103-01 g in 1 VIAL; Type 0: Not a Combination Product
    2NDC:44224-1103-33 in 1 BOX12/18/2025
    214 g in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01606/17/2025
    Labeler - Tender Corporation d/b/a Adventure Ready Brands (064437304)
    Establishment
    NameAddressID/FEIBusiness Operations
    Tender Corporation d/b/a Adventure Ready Brands064437304manufacture(44224-1103)
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