Label: HAND SANITIZER- alcohol gel

  • NDC Code(s): 70412-191-08, 70412-191-16
  • Packager: Zhejiang Ayan Biotech Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 6, 2023

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active Ingredients

    Ethyl Alcohol 62%

    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 a 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.  Harmful to wood finishes and plastics. o

  • Inactive Ingredients:

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

  • Package Labeling: 70412-191-08

    70412-191-08

  • Package Labeling: 70412-191-16

    70412-191-16

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70412-191
    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
    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:70412-191-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product04/20/2020
    2NDC:70412-191-16473 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(70412-191)