Label: GERMSTAR PREMIUM HAND SANITIZER- ethyl alcohol solution

  • NDC Code(s): 57915-008-01, 57915-008-02, 57915-008-03, 57915-008-04, view more
    57915-008-05
  • Packager: Soaptronic LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 6, 2023

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  • ACTIVE INGREDIENT

    Active ingredient

    Ethyl alcohol 63% (W/W)

  • PURPOSE

    Purpose

    Antiseptic

  • INDICATIONS & USAGE

    Uses


    Kills 99.99% of all disease causing germs on contact, and protects and restores moisture.

  • WARNINGS

    Warnings

    For external use only. Keep out of eyes. In case of eye contact immediately flush eyes with water. If irritation persists, get medical attention. If swallowed, contact physician. Flammable, keep away from heat or flames.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    Directions

    Apply Germstar all over the surface of your hands and rub into skin until dry. Supervise children in the use of this product.

  • SPL UNCLASSIFIED SECTION

    Other information

    Germstar is non allergenic. Store at 20° to 25°C (68° to 77°F). May be harmful to some surfaces/materials.

  • INACTIVE INGREDIENT

    Inactive ingredients

    Water, Isopropanol, Emollient Complex, Fragrance

  • QUESTIONS

    Questions?

    Call Germstar at 1-800.327.2606

  • PRINCIPAL DISPLAY PANEL

    57915-008-05.Tropical57915-008-04.Refresh57915-008-03.Pink57915-008-02.Juicy57915-008-01.Breeze

  • INGREDIENTS AND APPEARANCE
    GERMSTAR PREMIUM HAND SANITIZER 
    ethyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57915-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL630 g  in 1000 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57915-008-0159 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/01/2017
    2NDC:57915-008-0259 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/01/2017
    3NDC:57915-008-0359 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/01/2017
    4NDC:57915-008-0459 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/01/2017
    5NDC:57915-008-0559 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/01/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/01/2017
    Labeler - Soaptronic LLC (082741674)
    Registrant - Soaptronic, LLC (082741674)
    Establishment
    NameAddressID/FEIBusiness Operations
    Soaptronic, LLC082741674manufacture(57915-008)
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