Label: ANTI BACTERIAL HAND GEL SWEET CINNAMON PUMPKIN- alcohol gel

  • NDC Code(s): 62670-6666-0
  • Packager: Bath & Body Works, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated June 24, 2024

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

View All Sections
  • Active Ingredient

    Alcohol 71%

  • Purpose

    Antiseptic

  • Use

    Decreases bacteria on hands.

  • Warnings

    Flammable: Keep away from flame or high heat.

  • WARNINGS

    For external use only.

  • WHEN USING

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

  • KEEP OUT OF REACH OF CHILDREN

    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 INGREDIENT

    Water (Aqua, Eau), Fragrance (Parfum), Carbomer, Mannitol, Isopropyl Myristate, Cellulose, Hydroxyethyl Urea, Tocopheryl Acetate, Wheat Amino Acids, Aloe Barbadensis Leaf Juice, Butyrospermum Parkii (Shea) Butter Extract, Kaolin, Silica, Hydroxypropyl Methylcellulose, Caprylic/Capric Triglyceride, Retinyl Palmitate, Aminomethyl Propanol, Yellow 5 (CI 19140), Ultramarines (CI 77007), Red 33 (CI 17200), Ext. Violet 2 (CI 60730).

  • SPL UNCLASSIFIED SECTION

    Bath & Body Works, Distr., 95 West Main Street
    New Albany, OH 43054, 1-800-395-1001
    pat. www.bbwinc.com/patents

  • PRINCIPAL DISPLAY PANEL

    ABHG Sweet Cinnamon Pumpkin

  • INGREDIENTS AND APPEARANCE
    ANTI BACTERIAL HAND GEL  SWEET CINNAMON PUMPKIN
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62670-6666
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL71 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62670-6666-029 mL in 1 BOTTLE; Type 0: Not a Combination Product06/17/202406/17/2027
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/17/202406/17/2027
    Labeler - Bath & Body Works, Inc. (878952845)
    Establishment
    NameAddressID/FEIBusiness Operations
    KDC US Holdings, Inc.080783283manufacture(62670-6666)
    Establishment
    NameAddressID/FEIBusiness Operations
    Memphis Contract Packaging117443103manufacture(62670-6666)
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

More Info on this Drug

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