Label: ANTI-BACTERIAL HAND SANITIZER EUCALYPTUS SPEARMINT- 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 20, 2015

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

View All Sections
  • ACTIVE INGREDIENT

    Alcohol 68%

  • PURPOSE

    Antiseptic

  • USE

    Decrease bacteria on hands.

  • WARNINGS

    For external use only.

  • FLAMMABLE

    Keep away from flame or high heat.

  • WHEN USING THIS PRODUCT

    avoid contact with eyes.  If contact occurs, rinse thoroughly with water.

  • STOP USE AND ASK A DOCTOR

    if irritation and redness develop or increase.

  • 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), Eucalyptus Globulus Leaf Oil, Mentha Viridis (Spearmint) Leaf Oil, Honey Extract (Mel, Extrait de miel), Elaeis Guineensis (Palm) Extract, Cocos Nucifera (Coconut) Fruit Extract, Olea Europaea (Olive) Fruit Extract, Wheat Amino Acids, Retinyl Palmitate, Tocopheryl Acetate, Glycerin, Carbomer, Hydroxyethyl Urea, Hydroxypropyl Methylcellulose, Lactose, Aminomethyl Propanol, Isopropyl Myristate, Cellulose, Propylene Glycol, Ultramarines (CI 77007), Yellow 5 (CI 19140), Red 40 (CI 16035).

  • COMPANY INFORMATION

    Bath & Body Works, Distr.

    Reynoldsburg, Ohio 43068

    1-800-395-1001

    www.bathandbodyworks.com

  • PRODUCT PACKAGING

    MM1

  • INGREDIENTS AND APPEARANCE
    ANTI-BACTERIAL HAND SANITIZER  EUCALYPTUS SPEARMINT
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62670-4780
    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:62670-4780-3225 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/04/2014
    Labeler - Bath & Body Works, Inc. (878952845)
    Establishment
    NameAddressID/FEIBusiness Operations
    Knowlton Development Corporation968939913manufacture(62670-4780)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!