Label: DELTA GERM 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 January 5, 2021

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

View All Sections
  • Active Ingredients

    Ethyl Alcohol 62%v/v.

    Purpose: Antiseptic

  • Purpose

    Antiseptic

  • Uses

    • helps reduce bacteria on the skin that could cause disease
  • Directions

    • Place enough product in your palm to thoroughly cover your hands
    • Rub hands together briskly until dry
    • Children should be supervised when using this product.
    • For personal and occasional domestic use
  • Warnings

    For external use only.

    Flammable. Keep away from fire or flame.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Ask Doctor

    Stop Use and Ask a doctor if irritation or redness develops

  • Safety Instructions

    Flammable, Keep away from fire and flame

  • Other Information

    Store below 15-30°C

    May discolor certain fabrics or surfaces.

    Avoid freezing and excessive heat

  • Inactive Ingredients

    water, hydrolyzed jojoba esters, glycerin, Acrylates C10-30 Alkyl Acrylate Crosspolymer, fragrance, aminomethyl propanol, Vitamin E

  • PRINCIPAL DISPLAY PANEL

    Sani

  • INGREDIENTS AND APPEARANCE
    DELTA GERM HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79861-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)  
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79861-004-0660 mL in 1 BOTTLE; Type 0: Not a Combination Product01/05/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/05/2021
    Labeler - Sanihealth Labs Inc. (204172811)
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!