Label: ANTI-BACTERIAL HAND SANITIZER BLACK CHERRY MERLOT- 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 December 14, 2021

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

View All Sections
  • ACTIVE INGREDIENT

    Alcohol 71%

  • 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), Fragrance (Parfum), Carbomer, Lactose, Propylene Glycol, Aminomethyl Propanol, Isopropyl Myristate, Cellulose, Hydroxyethyl Urea, Tocopheryl Acetate, Wheat Amino Acids, Aloe Barbadensis Leaf Juice, Butyrospermum Parkii (Shea) Butter Extract, Hydroxypropyl Methylcellulose, Retinyl Palmitate, Ultramarines (CI 77007), Red 33 (CI 17200), 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

    AB HS Black Cherry Merlot

  • INGREDIENTS AND APPEARANCE
    ANTI-BACTERIAL HAND SANITIZER  BLACK CHERRY MERLOT
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62670-6198
    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:62670-6198-3225 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/14/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E12/14/2021
    Labeler - Bath & Body Works, Inc. (878952845)
    Establishment
    NameAddressID/FEIBusiness Operations
    KDC US Holdings, Inc.792844680manufacture(62670-6198)
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!