Label: SANITIZING HAND MIST - UNSCENTED- ethyl alcohol spray
SANITIZING HAND GEL - UNSCENTED- ethyl alcohol gel
SANITIZING HAND GEL - LEMONGRASS- ethyl alcohol gel
SANITIZING HAND MIST - PEPPERMINT EUCALYPTUS- ethyl alcohol spray
SANITIZING HAND MIST - LEMONGRASS- ethyl alcohol spray
SANITIZING HAND GEL - PEPPERMINT EUCALYPTUS- ethyl alcohol gel

  • NDC Code(s): 80588-010-02, 80588-010-08, 80588-011-02, 80588-011-08, view more
    80588-012-02, 80588-012-08, 80588-020-08, 80588-020-32, 80588-021-08, 80588-021-32, 80588-022-08, 80588-022-32
  • Packager: Alkaline Corporation
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated January 8, 2024

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  • Active Ingredients

    Ethyl Alcohol 70%

  • Purpose

    Antiseptic

  • Uses

    For handwashing to decrease bacteria on the skin

  • Warnings

    Flammable. Keep away from fire or flame. For external use only.

    When using this product

    Do not use in eyes. In case of contact with eyes, rinse with water.

    Stop use and ask a doctor if

    irritation and redness develop and persist.

    Keep out of reach of children.

    If swallowed, get medical help promptly.

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping.

  • Other information

    Store under 105°F

  • Inactive Ingredients

    NDC 80588-010:

    Water, Glycerine, Aloe Barbadensis Leaf

    NDC 80588-011:

    Water, Glycerine, Aloe Barbadensis Leaf, Eucalyptus Radiata Flower/Leaf/Stem Oil, Piper Mentha Piperita (Peppermint) Oil

    NDC 80588-012:

    Water, Glycerine, Aloe Barbadensis Leaf, Cymbopogon Schoenanthus (Lemongrass) Oil

    NDC 80588-020:

    Water, Glycerine, Rapidgel EZ, Aloe Barbadensis Leaf

    NDC 80588-011:

    Water, Glycerine, Rapidgel EZ, Aloe Barbadensis Leaf, Eucalyptus Radiata Flower/Leaf/Stem Oil, Piper Mentha Piperita (Peppermint) Oil

    NDC 80588-012:

    Water, Glycerine, Rapidgel EZ, Aloe Barbadensis Leaf, Cymbopogon Schoenanthus (Lemongrass) Oil

  • Sanitizing Hand Mist - Unscented + Aloe: NDC 80588-010-02

    NDC 80588-010-02

  • Sanitizing Hand Mist - Unscented + Aloe: NDC 80588-010-08

    NDC 80588-010-08

  • Sanitizing Hand Mist - Peppermint Eucalyptus + Aloe: NDC 80588-011-02

    NDC 80588-011-02

  • Sanitizing Hand Mist - Peppermint Eucalyptus + Aloe: NDC 80588-011-08

    NDC 80588-011-08

  • Sanitizing Hand Mist - Lemongrass + Aloe: NDC 80588-012-02

    NDC 80588-012-02

  • Sanitizing Hand Mist - Lemongrass + Aloe: NDC 80588-012-08

    NDC 80588-012-08

  • Sanitizing Hand Gel - Unscented + Aloe: NDC 80588-020-08

    NDC 80588-020-08

  • Sanitizing Hand Gel - Unscented + Aloe: NDC 80588-020-32

    NDC 80588-020-32

  • Sanitizing Hand Gel - Peppermint Eucalyptus + Aloe: NDC 80588-021-08

    NDC 80588-021-08

  • Sanitizing Hand Gel - Peppermint Eucalyptus + Aloe: NDC 80588-021-32

    NDC 80588-021-32

  • Sanitizing Hand Gel - Lemongrass + Aloe: NDC 80588-022-08

    NDC 80588-022-08

  • Sanitizing Hand Gel - Lemongrass + Aloe: NDC 80588-022-32

    NDC 80588-022-32

  • INGREDIENTS AND APPEARANCE
    SANITIZING HAND MIST - UNSCENTED 
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80588-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE (UNII: V5VD430YW9)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80588-010-0259 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/09/2022
    2NDC:80588-010-08236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/09/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/09/2022
    SANITIZING HAND GEL - UNSCENTED 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80588-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE (UNII: V5VD430YW9)  
    ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80588-020-08236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/09/2022
    2NDC:80588-020-32900 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product06/09/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/09/2022
    SANITIZING HAND GEL - LEMONGRASS 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80588-022
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE (UNII: V5VD430YW9)  
    ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80588-022-08236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/09/2022
    2NDC:80588-022-32900 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product06/09/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/09/2022
    SANITIZING HAND MIST - PEPPERMINT EUCALYPTUS 
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80588-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE (UNII: V5VD430YW9)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80588-011-0259 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/09/2022
    2NDC:80588-011-08236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/09/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/09/2022
    SANITIZING HAND MIST - LEMONGRASS 
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80588-012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE (UNII: V5VD430YW9)  
    EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80588-012-0259 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/09/2022
    2NDC:80588-012-08236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/09/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/09/2022
    SANITIZING HAND GEL - PEPPERMINT EUCALYPTUS 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80588-021
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE (UNII: V5VD430YW9)  
    ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80588-021-08236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/09/2022
    2NDC:80588-021-32900 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product06/09/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/09/2022
    Labeler - Alkaline Corporation (790098318)
    Establishment
    NameAddressID/FEIBusiness Operations
    Alkaline Corporation790098318manufacture(80588-010, 80588-011, 80588-012, 80588-020, 80588-021, 80588-022) , pack(80588-010, 80588-011, 80588-012, 80588-020, 80588-021, 80588-022) , label(80588-010, 80588-011, 80588-012, 80588-020, 80588-021, 80588-022)
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