Label: HAND SANITIZER- sda 40b alcohol 200 proof liquid

  • NDC Code(s): 52854-600-01, 52854-600-02, 52854-600-03, 52854-600-04, view more
    52854-600-05, 52854-600-06
  • Packager: Tropical Seas, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 1, 2024

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  • Drug Facts

    Drug Facts

  • Active Ingredients

    Ethyl Alcohol 64.325%

  • Purpose

    Antiseptic

  • Uses

    • for sanitizing hands to help reduce bacteria on the skin.
    • for deodorizing hands to help reduce odors on the skin.
  • Warnings

    For external use only

    Do not use on damaged or broken skin

    When using this product keep out of eyes. Rinse with water to remove.

    Stop use and ask a doctor if rash occurs

    Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • rinse solids & slime from hands if possible.
    • pat dry.
    • put a thumbnail size amount in your palm and rub hands together briskly until dry.
    • repeat as needed.
    • children under 6 months: As a doctor
  • Inactive Ingredients

    deionized water, glycerin, acrylates/c10-30 alkyl acrylate crosspolymer, aminomethyl propanol, and fragrance.

  • Other Information

    Warning: Flammable

    • do not use near open flame or heat source
    • do not store above 110°F (43°C)
    • protect this product from excessive heat and direct sun
    • may discolor certain fabrics or surfaces
  • Questions or Comments?

    Call toll free1-800-368-7327

  • Principal Display Panel - Bottle Label

    60ml NDC: 52854-600-01 60ml label

    119ml NDC: 52854-600-02 119ml label

    237ml NDC: 52854-600-03 237ml label

    250ml NDC: 52854-600-04 250ml label

    1000ml NDC: 52854-600-05 1000ml label

    3785ml NDC: 52854-600-06 3785ml label

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    sda 40b alcohol 200 proof liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52854-600
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL64.325 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52854-600-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product03/28/2009
    2NDC:52854-600-02119 mL in 1 BOTTLE; Type 0: Not a Combination Product03/28/2009
    3NDC:52854-600-03237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/28/2009
    4NDC:52854-600-04250 mL in 1 BOTTLE; Type 0: Not a Combination Product03/28/2009
    5NDC:52854-600-051000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/28/2009
    6NDC:52854-600-063785 mL in 1 JUG; Type 0: Not a Combination Product03/28/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/28/2009
    Labeler - Tropical Seas, Inc. (627865660)
    Establishment
    NameAddressID/FEIBusiness Operations
    Tropical Seas, Inc.627865660manufacture(52854-600)
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