Label: GERM OUT HAND SANITIZER- ethyl alcohol gel

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated June 9, 2020

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

  • Active Ingredients

    Ethyl Alcohol 70% v/v.................Antiseptic

  • Purpose

    Antiseptic

  • Use

    hand sanitizer to help reduce bacteria on the skin

  • Safety Instructions

    Flammable, Keep away from fire and flame

  • When using this product

    In case of contact,rinse eyes thoroughly with water

  • Do not use

    Do  not use in or near eyes.

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, get medical help or contact Poison Control  center right away.

  • Other Information

    Store below 110°F (43°C)
    May discolor certain fabrics or surfaces.

  • Inactive Ingredients

    Water (aqua), Triethanolamine, Carbomer, Fragrance, Glycerin. Propylene Glycol.

  • Directions

    • apply palmful to hands.
    • rub hands together vigorously until dry.
    • supervise children in the use of this product.
  • PRINCIPAL DISPLAY PANEL

    germout1

  • INGREDIENTS AND APPEARANCE
    GERM OUT HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72308-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72308-006-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product06/09/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/09/2020
    Labeler - Flex Beauty Labs (080858917)