Label: INSTANT HAND SANITIZER- alcohol gel

  • NDC Code(s): 77573-002-01, 77573-002-02, 77573-002-03
  • Packager: JIANGSU AIMEILI COSMETIC CO.,LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 5, 2024

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

  • Active Ingredient(s)

    ethanol 75% (v/v) Purpose: Antiseptic

  • Purpose

    Antiseptic

  • Use

    to decrease bacteria on the skin that could cause disease

    recommended for repeated use

    use without water

  • Warnings

    For external use only.

    Flammable. Keep away from heat or flame

    discontinue if skin becomes irritated and ask a doctor

    keep out of reach of children, in case of accodental igestion,seek prefessional assistance or contact a poison control center immediately

  • DO NOT USE

    do not inhale or ingest

    do not use on open skin wounds.

  • when using this product

    keep out of eyes.In case of contacting with eyes,flush thoroughly with water.

    do not inhale or ingest

    do not use on open skin wounds

  • STOP USE

    discontine of skin becomes irritated and ask a doctor.

    Keep out of reach of children,in case of accidental ingestion,seek professional assistance or contact a poison control center immediately

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. in case of accidental ingestion,seek professional assistance or contact a poison control center immediately.

  • Directions

    wet hands thoughly with product and rub until dry without wiping

    for children under 6,use only under adult supervision

    not recommended for infants

  • Other information

    do not store above 105℉

    may discolor some fabrics

  • Inactive ingredients

    Aqua,Aloe extract, triethanolamine,glycerin,carbomer,vitamin E

  • Package Label - Principal Display Panel

    label

  • INGREDIENTS AND APPEARANCE
    INSTANT HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77573-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) 1 mL  in 100 mL
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 2 mL  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.1 mL  in 100 mL
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) 0.25 mL  in 100 mL
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK) 0.25 mL  in 100 mL
    HYDANTOIN (UNII: I6208298TA) 0.2 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77573-002-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product07/03/2020
    2NDC:77573-002-02100 mL in 1 BOTTLE; Type 0: Not a Combination Product07/03/2020
    3NDC:77573-002-03500 mL in 1 BOTTLE; Type 0: Not a Combination Product07/03/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00507/03/2020
    Labeler - JIANGSU AIMEILI COSMETIC CO.,LTD (543903077)
    Establishment
    NameAddressID/FEIBusiness Operations
    JIANGSU AIMEILI COSMETIC CO.,LTD543903077manufacture(77573-002)