Label: ANTI-BACTERIAL HAND EUCALYPTUS SPEARMINT- alcohol gel

  • NDC Code(s): 62670-5912-0, 62670-5912-1, 62670-5912-3
  • Packager: Bath & Body Works, Inc.
  • Category: HUMAN OTC DRUG LABEL

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 November 11, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    Alcohol 71%

  • 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), Fragrance (Parfum), Carbomer, Lactose, Aminomethyl Propanol, Isopropyl Myristate, Cellulose, Propylene Glycol, Hydroxyethyl Urea, Tocopheryl Acetate, Wheat Amino Acids, Aloe Barbadensis Leaf Juice, Butyrospermum Parkii (Shea) Butter Extract, Hydroxypropyl Methylcellulose, Retinyl Palmitate, Ultramarines (CI 77007), Ext. Violet 2 (CI 60730), Yellow 5 (CI 19140).

  • COMPANY INFORMATION

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

  • PRODUCT PACKAGING

    ABHG Eucalyptus Spearmint

  • INGREDIENTS AND APPEARANCE
    ANTI-BACTERIAL HAND   EUCALYPTUS SPEARMINT
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62670-5912
    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:62670-5912-029 mL in 1 BOTTLE; Type 0: Not a Combination Product11/11/2020
    2NDC:62670-5912-173 mL in 1 BOTTLE; Type 0: Not a Combination Product11/11/2020
    3NDC:62670-5912-3225 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E11/11/2020
    Labeler - Bath & Body Works, Inc. (878952845)