Label: INSIGNIA INSTANT HAND SANITIZER- alcohol solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated June 8, 2020

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  • Active Ingredient(s)

    Ethyl Alcohol 80% v/v

  • Purpose

    Antiseptic

  • Use

    To decrease bacteria on the skin that could cause disease

    Recommended for repeated use

    To use anywhere without water

  • Warnings

    For external use only. Flammable. Keep away from heat and flame

    Discontinue if skin becomes irritated and ask a doctor

  • WHEN USING

    When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water.

    Do not inhale or ingest

    Avoid contact with broken skin

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of accidental ingest, seek professional assist or contact a Poison Control Center immediately.

  • Directions

    • Wet hands thoroughly 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 40C (104F)
    • May discolor wood or fabrics
    • Harmful to wood finishes or plastics
  • Inactive ingredients

    Carbomer, Triethanolamine, Glycerin, PEG-7 glyceryl CoCoate, Water, Parfum (Fragrance), Aloe barbadensis leaf extract

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    INSIGNIA INSTANT HAND SANITIZER 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75410-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER 934 (UNII: Z135WT9208)  
    TRIETHANOLAMINE SULFATE (UNII: MV1V89M17O)  
    PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75410-003-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product06/08/2020
    2NDC:75410-003-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product06/08/2020
    3NDC:75410-003-03100 mL in 1 BOTTLE; Type 0: Not a Combination Product06/08/2020
    4NDC:75410-003-04250 mL in 1 BOTTLE; Type 0: Not a Combination Product06/08/2020
    5NDC:75410-003-05500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/08/2020
    6NDC:75410-003-061000 mL in 1 BOTTLE; Type 0: Not a Combination Product06/08/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/08/2020
    Labeler - Yiwu Story of Love Cosmetic Co., Ltd (679768544)
    Establishment
    NameAddressID/FEIBusiness Operations
    Yiwu Story of Love Cosmetic Co., Ltd679768544manufacture(75410-003)
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