Label: ANTI-BACTERIAL HAND FRENCH LAVENDER- 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 June 29, 2018

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  • ACTIVE INGREDIENT

    Alcohol 68%

  • PURPOSE

    Antiseptic

  • USE

    Decreases 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), Carbomer, Citrus Limon (Lemon) Peel Oil, Aminomethyl Propanol, Isopropyl Myristate, Propylene Glycol, Hydroxyethyl Urea, Lavandula Angustifolia (Lavender) Oil, Wheat Amino Acids, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Glycerin, Honey Extract (Mel, Extrait de miel), Elaeis Guineensis (Palm) Extract, Cocos Nucifera (Coconut) Fruit Extract, Olea Europaea (Olive) Fruit Extract, Red 33 (CI 17200), Blue 1 (CI 42090), Ext. Violet 2 (CI 60730), Yellow 5 (CI 19140).

  • COMPANY INFORMATION

    Bath & Body Works, Distr., 95 West Main Street

    New Albany, OH, 43054, 1-800-395-1001

    Shop 24/7 at www.bathandbodyworks.com

  • PRODUCT PACKAGING

    AB HG French Lavender

  • INGREDIENTS AND APPEARANCE
    ANTI-BACTERIAL HAND  FRENCH LAVENDER
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62670-5442
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL68 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62670-5442-029 mL in 1 BOTTLE; Type 0: Not a Combination Product06/29/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/29/2018
    Labeler - Bath & Body Works, Inc. (878952845)
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