Label: HAND SANITIZER PLUS- alcohol gel

  • NDC Code(s): 63742-040-00, 63742-040-01
  • Packager: Clinical Resolution Laboratory, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 26, 2023

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  • DRUG FACTS

  • Active Ingredient

    Ethyl Alcohol 70% v/v

    Purpose

    Antiseptic

  • Uses:

    • To decrease bacteria on the skin that could cause disease.
    • Recommended for repeated use.
  • Warnings:

    For external use only: Hands

    Flammable, keep away from fire or flame.

    When using this product

    • Keep out of eyes. In case of contact with eyes, rinse thoroughly with water.
    • Avoid contact with broken skin.
    • Do not inhale or ingest.

    Stop use and ask a doctor if

    • Irritation and redness develop.
    • Condition persists for more than 72 hours.

    Keep out of reach of children

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

  • Directions

    • Wet hands thoroughly with product and allow to dry without wiping.
    • For children under 6, use only under adult supervision.
    • Not recommended for infants.
  • Other information

    • Do not store above 105°F.
    • May discolor some fabrics or surfaces.
    • Harmful to wood finishes and plastics.
  • Inactive Ingredients

    Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Vera Leaf Juice, Aminomethyl Propanol, Fragrance, Glycerin, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Isopropyl Alcohol, Isopropyl Myristate, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Tocopheryl Acetate, Water

  • Package Labeling:

    Label

  • Package Labeling: 60ml

    Label2

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER PLUS 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63742-040
    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
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63742-040-00118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2020
    2NDC:63742-040-0160 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/01/2020
    Labeler - Clinical Resolution Laboratory, Inc. (825047942)
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