Label: HAND SANITIZER- alcohol gel

  • NDC Code(s): 70412-192-36
  • Packager: Zhejiang Ayan Biotech Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 6, 2023

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

  • Drug Facts

  • Active Ingredients

    Ethyl Alcohol 70% v/v

    Purpose

    Antiseptic

  • Uses:

    For Hand Sanitizing

  • Warnings:

    For external use only-hands.

    Keep away from heat and flame. Flammable. 

    When using this product

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

    Stop use and ask a doctor

    if skin irritation develops.

    Keep out of reach of children.

    If swallowed, get medical help or call 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 fabricsHarmful to wood finishes and plastics.

  • Inactive Ingredients:

    Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl ACetate, Triethanomalime, Water.

  • Package Labeling:

    70412-192-36

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70412-192
    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 HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70412-192-36236 mL in 1 BOTTLE; Type 0: Not a Combination Product04/20/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/20/2020
    Labeler - Zhejiang Ayan Biotech Co.,Ltd. (544377996)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Ayan Biotech Co.,Ltd.544377996manufacture(70412-192)