Label: ANTI-BACTERIALHANDSPRAY WINTER CANDY APPLE- alcohol spray

  • NDC Code(s): 62670-6986-2
  • Packager: Bath & Body Works, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 10, 2026

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  • 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 if irritation and redness develop.

  • 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

    Water (Aqua, Eau), Fragrance (Parfum), PEG-12 Dimethicone, Butyrospermum Parkii (Shea) Butter Extract, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Hexamethylindanopyran, Citrus Aurantium Peel Oil, Limonene, Hexyl Cinnamal, Vanillin, Citronellol, Linalool, Acetyl Cedrene, Tetramethyl Acetyloctahydronaphthalenes, Geranyl Acetate, Amyl Cinnamal, Geraniol, Terpineol, Benzyl Salicylate, Eugen, Red 40 (CI 16035), Red 33 (CI 17200), Yellow 5 (CI 19140), 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

    ABHS Winter Candy Apple

  • INGREDIENTS AND APPEARANCE
    ANTI-BACTERIALHANDSPRAY  WINTER CANDY APPLE
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62670-6986
    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:62670-6986-229 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product10/20/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/20/2025
    Labeler - Bath & Body Works, Inc. (878952845)
    Establishment
    NameAddressID/FEIBusiness Operations
    Tri Tech Laboratories LLC117211775manufacture(62670-6986)
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