Label: HAND SANITIZER USA liquid
HAND SANITIZER- alcohol liquid

  • Contains inactivated NDC Code(s)
    NDC Code(s):
    74010-3010-1, 74010-3010-2, 74010-3010-3, 74010-3010-4, view more
    74010-3010-5, 74010-3010-6, 74010-3016-1, 74010-3016-2, 74010-3016-3, 74010-3016-4, 74010-3016-5, 74010-3016-6
  • Packager: Global Universal SRL LLC dba Minhas Micro Distillery
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

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 April 7, 2020

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

  • Hand Sanitizer EXPORT

    74010-3010-6 Export 750 FRONT74010-3010-6 EXPORT 750 BACK74010-3010-4 EXPORT 1000 74010-3010-3 EXPORT 375 FRONT74010-3010-3 EXPORT 375 BACK74010-3010-1 EXPORT 50ML74010-3010-2 EXPORT 200ML FRONT74010-3010-2 EXPORT 200ML BACK74010-3010-5 EXPORT 1140 FRONT74010-3010-5 EXPORT 1140 BACK

  • Hand Sanitizer USA

    USA Made Sold USA Hand Sanitizer 50 mlUSA Made Sold USA Hand San 200 mlUSA Made Sold USA Hand San 375 mlUSA Made Sold USA Hand San 750mlUSA Made Sold USA Hand San 1000 mlUSA Made Sold USA Hand San 1140 ml

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER USA 
    hand sanitizer usa liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74010-3016
    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
    DENATONIUM BENZOATE ANHYDROUS (UNII: M5BA6GAF1O)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Colorwhite (clear liquid) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74010-3016-150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
    2NDC:74010-3016-2200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
    3NDC:74010-3016-51000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
    4NDC:74010-3016-3375 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
    5NDC:74010-3016-61140 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
    6NDC:74010-3016-4750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/26/2020
    HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74010-3010
    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
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Product Characteristics
    Colorwhite (clear liquid) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74010-3010-150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/29/2020
    2NDC:74010-3010-2200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
    3NDC:74010-3010-41000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
    4NDC:74010-3010-3375 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
    5NDC:74010-3010-51140 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
    6NDC:74010-3010-6750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Export only03/26/2020
    Labeler - Global Universal SRL LLC dba Minhas Micro Distillery (066395536)
    Establishment
    NameAddressID/FEIBusiness Operations
    Global Universal SRL LLC dba Minhas Micro Distillery066395536manufacture(74010-3016, 74010-3010) , repack(74010-3016, 74010-3010)