PURELL ADVANCED HYGIENIC HAND RUB (ALCOHOL) GEL [GOJO INDUSTRIES, INC.]

PURELL ADVANCED HYGIENIC HAND RUB (ALCOHOL) GEL [GOJO INDUSTRIES, INC.]
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NDC 21749-752-01, 21749-752-02, 21749-752-04, 21749-752-10, 21749-752-12, 21749-752-16, 21749-752-80, 21749-752-89, 21749-752-97
Set ID 5008e33b-880c-4ab9-b9b0-37ae8992df7a
Category HUMAN OTC DRUG LABEL
Packager GOJO Industries, Inc.
Generic Name
Product Class
Product Number
Application Number
  • PRINCIPAL DISPLAY PANEL

    Product LabelProduct LabelProduct Label

  • INGREDIENTS AND APPEARANCE
    PURELL ADVANCED HYGIENIC HAND RUB 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-752
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Isopropyl Alcohol (UNII: ND2M416302)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-752-0130 mL in 1 PACKAGE; Type 0: Not a Combination Product08/15/2012
    2NDC:21749-752-0260 mL in 1 PACKAGE; Type 0: Not a Combination Product08/15/2012
    3NDC:21749-752-04118 mL in 1 PACKAGE; Type 0: Not a Combination Product08/15/2012
    4NDC:21749-752-12350 mL in 1 PACKAGE; Type 0: Not a Combination Product08/15/2012
    5NDC:21749-752-16450 mL in 1 PACKAGE; Type 0: Not a Combination Product01/30/2016
    6NDC:21749-752-97700 mL in 1 PACKAGE; Type 0: Not a Combination Product01/30/2012
    7NDC:21749-752-80800 mL in 1 PACKAGE; Type 0: Not a Combination Product08/15/2012
    8NDC:21749-752-101000 mL in 1 PACKAGE; Type 0: Not a Combination Product08/15/2012
    9NDC:21749-752-891200 mL in 1 PACKAGE; Type 0: Not a Combination Product01/30/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    export only01/30/2012
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-752)

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