Label: ANTI-BACTERIAL HAND GEL BRIGHT CHRISTMAS MORNING- alcohol gel

  • NDC Code(s): 62670-6546-0
  • Packager: Bath & Body Works, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 24, 2023

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  • Active Ingredient

    Alcohol 71%

  • Purpose

    Antiseptic

  • Use

    Decreases bacteria on hands.

  • Warnings

    Flammable: Keep away from flame or high heat.

  • WARNINGS

    For external use only.

  • WHEN USING

    When using this product keep out of eyes. Stop use and ask a doctor if irritation or redness develops.

  • 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

    Rub a dime sized drop into hands.

  • INACTIVE INGREDIENT


    Inactive Ingredients: Water (Aqua, Eau),
    Fragrance (Parfum), Carbomer, Propylene Glycol,
    Lactose, Aminomethyl Propanol, Isopropyl
    Myristate, Cellulose, Hydroxyethyl Urea, Tocopheryl
    Acetate, Wheat Amino Acids, Aloe Barbadensis Leaf
    Juice, Butyrospermum Parkii (Shea) Butter
    Extract, Hydroxypropyl Methylcellulose, Retinyl
    Palmitate, Ultramarines (CI 77007), Red 40
    (CI 16035), Red 33 (CI 17200), Yellow 5
    (CI 19140), Ext. Violet 2 (CI 60730).

  • SPL UNCLASSIFIED SECTION

    Bath & Body Works, Distr., 95 West Main Street
    New Albany, OH 43054, 1-800-395-1001
    pat. www.bbwinc.com/patents

  • PRINCIPAL DISPLAY PANEL

    ABHG Bright Christmas Morning

  • INGREDIENTS AND APPEARANCE
    ANTI-BACTERIAL HAND GEL  BRIGHT CHRISTMAS MORNING
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62670-6546
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL71 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62670-6546-029 mL in 1 BOTTLE; Type 0: Not a Combination Product10/23/202310/23/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/23/202310/23/2025
    Labeler - Bath & Body Works, Inc. (878952845)
    Establishment
    NameAddressID/FEIBusiness Operations
    KDC US Holdings, Inc.080783283manufacture(62670-6546)
    Establishment
    NameAddressID/FEIBusiness Operations
    Memphis Contract Packaging117443103manufacture(62670-6546)
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