Label: ANTI-BACTERIAL HAND- alcohol gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 1, 2010

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  • ACTIVE INGREDIENT

    Alcohol 68%

  • PURPOSE

    Antiseptic

  • USE

    Decrease bacteria on hands.

  • WARNINGS

    For external use only.

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


  • FLAMMABLE

    Keep away from flame or high heat.

  • 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 INGREDIENTS

    Water (Aqua, Eau), Isopropyl Alcohol,  Fragrance (Parfum), Honey Extract (Mel, Extrait de Miel), Elaeis Guineensis (Palm) Extract,  Olea Europaea (Olive) Fruit Extract, Cocos Nucifera (Coconut) Fruit Extract, Wheat Amino Acids, Retinyl Palmitate, Tocopheryl Acetate, Glycerin, Carbomer, Cellulose, Hydroxyethyl Urea, Hydroxypropyl Methylcellulose, Lactose, Isopropyl Myristate, Propylene Glycol, Aminomethyl Propanol, Ultramarines (CI 77007), Yellow 5 (CI 19140), Red 33 (CI 17200), Blue 1 (CI 42090).

  • COMPANY INFORMATION

    Bath & Body Works, Distr.
    Reynoldsburg, Ohio 43068
    1-800-395-1001
    www.bathandbodyworks.com

  • PRODUCT PACKAGING

    Front Label
    Back Label
  • INGREDIENTS AND APPEARANCE
    ANTI-BACTERIAL HAND   WARM VANILLA SUGAR
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62670-3643
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL68 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62670-3643-029 mL in 1 BOTTLE
    2NDC:62670-3643-173 mL in 1 BOTTLE
    3NDC:62670-3643-3236 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/01/2010
    Labeler - Bath & Body Works, Inc. (878952845)
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