Label: ANTI-BACTERIAL HAND FRENCH LAVENDER- alcohol gel

  • NDC Code(s): 62670-5650-0, 62670-5650-1, 62670-5650-3
  • Packager: Bath & Body Works, Inc.
  • 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 19, 2019

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

  • ACTIVE INGREDIENT

    Alcohol 68%

    Close
  • PURPOSE

    Antiseptic

    Close
  • USE

    Decrease bacteria on hands.

    Close
  • WARNINGS

    For external use only.

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


    Close
  • FLAMMABLE

    Keep away from flame or high heat.

    Close
  • KEEP OUT OF REACH OF CHILDREN

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

    Close
  • DIRECTIONS

    • Rub a dime sized drop into hands.
    Close
  • INACTIVE INGREDIENTS

    Water (Aqua, Eau), Isopropyl
    Alcohol, Fragrance (Parfum), Carbomer, Lactose,
    Aminomethyl Propanol, Isopropyl Myristate, Cellulose,
    Propylene Glycol, Hydroxyethyl Urea, Wheat Amino Acids,
    Tocopheryl Acetate, Retinyl Palmitate, Glycerin,
    Hydroxypropyl Methylcellulose, Aloe Barbadensis Leaf
    Juice, Elaeis Guineensis (Palm) Extract, Olea Europaea
    (Olive) Fruit Extract, Honey Extract (Mel, Extrait de miel),
    Cocos Nucifera (Coconut) Fruit Extract, Ultramarines
    (CI 77007), Red 33 (CI 17200), Yellow 5 (CI 19140),
    Blue 1 (CI 42090), Ext. Violet 2 (CI 60730).

    Close
  • COMPANY INFORMATION

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

    Close
  • PRODUCT PACKAGING
  • INGREDIENTS AND APPEARANCE
    ANTI-BACTERIAL HAND   FRENCH LAVENDER
    alcohol gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:62670-5650
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 68 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:62670-5650-0 29 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/19/2019
    2 NDC:62670-5650-1 73 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/19/2019
    3 NDC:62670-5650-3 236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 06/19/2019
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 06/19/2019
    Labeler - Bath & Body Works, Inc. (878952845)
    Close