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

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  • Active Ingredients

    Ethyl Alcohol 70% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic

  • Use

    hand sanitizer to help reduce bacteria on the skin

  • Safety Instructions

    Flammable, Keep away from fire and flame

  • When usinng this product

    do not  use in or near eyes. In case of contact, rinse eyes thoroghly with water.

  • Stop using 

    Stop use and ask a doctor  if irritation or redness develops.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Other Information

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

  • Inactive Ingredients

    Water (aqua), Triethanolamine, Carbomer, Aloe Barbadensis (Aloe Vera) Gel, Fragrance, Glycerin. Propylene Glycol. Tocopheryl Acetate (Vitamin E)

  • Directions

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

    germout3

  • INGREDIENTS AND APPEARANCE
    GERM OUT HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72308-008
    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)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72308-008-01236 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)