Label: BROMPTON AND LANGLEY MOISTURIZING HAND SANITIZER LAVNDER VANILLA- alcohol gel

  • NDC Code(s): 56136-730-01
  • Packager: Ganzhou Olivee Cosmetic Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 19, 2023

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

  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 70% 

  • Purpose

     Antiseptic

  • Use

    Antiseptic Cleanser, helps decrease bacteria on skin.

  • Warnings

    For external use only.

    Flammable. Keep product away from fire or flame.

    When using this product avoid contact with eyes. In case of contact flush eyes with water.

    Stop use and ask a doctor if irritation orredness develops and persists.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Spray a thumbnail size amount of product into your palm.
    • Rub hands together gently making sure to cover all areas of hands, air dry.
    • Children under 6 years of age should be supervised when using this product.
  • Inactive ingredients

    Water (Aqua), Glycerin, Fragrance (Parfum), Aloe Barbadensis leaf Extract, Tocopheryl Acetate (Vitamin E), Benzyl Salicylate, Limonene, Linalool.

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    BROMPTON AND LANGLEY MOISTURIZING HAND SANITIZER LAVNDER VANILLA 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56136-730
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:56136-730-0115 mL in 1 BOTTLE; Type 0: Not a Combination Product10/16/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00310/16/2023
    Labeler - Ganzhou Olivee Cosmetic Co., Ltd. (543008195)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ganzhou Olivee Cosmetic Co., Ltd.543008195manufacture(56136-730)