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

Drug Label Information

Updated November 1, 2024

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

View All Sections
  • 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)
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!