Label: ANTIBACTERIALHANDSPRAY AFTERNOON APPLE PICKING- alcohol spray

  • NDC Code(s): 62670-6600-0
  • Packager: Bath & Body Works, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 15, 2023

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

View All Sections
  • Active Ingredient

    Alcohol 72%

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

  • STOP USE

    Stop use and ask a doctor is irritation and redness develop or increase.

  • 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

    • Spray hands thoroughly.
    • Rub until dry.
  • INACTIVE INGREDIENT

    Inactive Ingredients: Water (Aqua, Eau), Fragrance (Parfum), PEG-12 Dimethicone, Propylene Glycol, Tocopheryl Acetate, Butyrospermum Parkii (Shea) Butter Extract, Aloe Barbadensis Leaf Juice, Red 40 (CI 16035), Ext. Violet 2 (CI 60730), Yellow 5 (CI 19140), Red 33 (CI 17200).

  • 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

    ABHS Afternoon Apple Picking

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIALHANDSPRAY  AFTERNOON APPLE PICKING
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62670-6600
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL72 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62670-6600-088 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/15/202311/15/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/15/202311/15/2026
    Labeler - Bath & Body Works, Inc. (878952845)
    Establishment
    NameAddressID/FEIBusiness Operations
    KDC US Holdings, Inc.080783283manufacture(62670-6600)
    Establishment
    NameAddressID/FEIBusiness Operations
    MCP TN117443103manufacture(62670-6600)
    Establishment
    NameAddressID/FEIBusiness Operations
    KDC US Holdings, Inc. (Groveport)118156334manufacture(62670-6600)
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!