Label: AFTER BITE KIDS- sodium bicarbonate cream

  • NDC Code(s): 90107-1280-1
  • Packager: Adventure Ready Brands
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 16, 2024

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

  • Drug Facts

  • Active Ingredient

    Sodium Bicarbonate (Baking Soda) 5%

  • Purpose

    Skin Protectant

  • Uses

    Temporarily protects and helps relieve minor skin irritation and itching due to

    • Insect bites
    • Poison ivy, oak, or sumac
  • Warnings

    for external use only..

  • When using this product

    do not get into eyes

  • Stop use and ask a doctor if

    • condition worsens
    • symptoms last more than 7 days or clear up and occur again within a few days
  • Keep Out of Reach of Children.

    If swallowed, get medical help or contact a Poison Control Center right away.
    If in eyes flush with water for 15 minutes and call a doctor.

  • Directions

    Use cap to puncture safety seal.

    • Adults and children 2 years and older for use as a cream, apply to the affected area of the skin as needed or as directed by a doctor
    • Children under 2 years ask a doctor
  • Inactive Ingredients

    Aloe Vera, Dimethicone, Emulsifying Wax, Eucalyptus Oil, Oleth-3 Phosphate, Oleth-10 Phosphate, Purified Water, Sodium Hydroxide, Tea Tree Oil and Vitamin E Acetate

  • Package Label

    Box

  • INGREDIENTS AND APPEARANCE
    AFTER BITE KIDS 
    sodium bicarbonate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:90107-1280
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM BICARBONATE1 g  in 20 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 1.1 g  in 20 g
    DIMETHICONE (UNII: 92RU3N3Y1O) 0.1 g  in 20 g
    EUCALYPTUS OIL (UNII: 2R04ONI662) 0.26 g  in 20 g
    OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL) 0.5 g  in 20 g
    OLETH-10 PHOSPHATE (UNII: Q95361F4VS) 0.28 g  in 20 g
    WATER (UNII: 059QF0KO0R) 14.1 g  in 20 g
    SODIUM HYDROXIDE (UNII: 55X04QC32I) 0.24 g  in 20 g
    TEA TREE OIL (UNII: VIF565UC2G) 0.2 g  in 20 g
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.1 g  in 20 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:90107-1280-11 in 1 BOX09/01/2020
    120 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01609/01/2020
    Labeler - Adventure Ready Brands (064437304)