Label: HAND SANITIZER- alcohol liquid

  • NDC Code(s): 74979-001-30, 74979-001-50
  • Packager: Robert Gordon Ind. Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 9, 2024

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  • Drug Facts

  • Active ingredient

    Alcohol 75%

    Purpose

    Antiseptic

  • Use

    • For hand washing to decrease bacteria on the skin
  • Warnings

    For External Use Only.

    • Flammable, keep away from fire and flame
    • Does not contain grain alcohol; do not drink.  If taken internally will produce serious gastric disturbances.

    When using this product

    • Avoid the eyes and mucous membranes
    •  In case of eyes or mucous membranes contact, rinse area thoroughly with water

    Stop use and ask a doctor if

    • Condition worsens
    • Redness or irritation develops
    • Condition persists for more than 3 days

    Keep out of reach of children.

    • If swallowed, contact a doctor or Poison Control Center immediately.
  • Directions

    • Rub dime sized amount between hands until dry.
    • Supervise children in the use of this product.
    • In the case of eye contact, rinse eyes thoroughly with wtaer.
  • ​Other information

    • Store below 105 oF
    • May discolor some fabrics.
  • Inactive Ingredients

    Water, Glycerin, Propylene Glycol, Fragrance, Carbomer, Aminomethyl propanol, Microcrystalline Cellulose, Lactose, Corn Starch Modified, Jojoba Esters, Ultramarines, FD&C Yellow No. 5, FD&C Blue No. 1

  • ​Questions?

    • 516-354-8888
  • Package Labeling: 30mL 74979-001-30

    30mL

  • Package Labeling: 50mL 74979-001-50

    50mL

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74979-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74979-001-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product05/20/2020
    2NDC:74979-001-5050 mL in 1 BOTTLE; Type 0: Not a Combination Product05/20/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/20/2020
    Labeler - Robert Gordon Ind. Ltd. (070064709)
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