Label: G AND H PROTECT HAND- benzalkonium chloride soap

  • NDC Code(s): 10056-026-00
  • Packager: Access Business Group LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 23, 2023

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  • Drug Facts

  • Active ingredient

    Benzalkonium Chloride 0.10%

    Purpose

    Antibacterial

  • Uses

    Helps reduce bacteria on hands.

  • Warnings

    For external use only.

    When using this product

    avoid contact with eyes. In case of contact, rinse thoroughly with water.

    Stop use and ask a doctor

    if irritation develops. These may be signs of a serious condition.

    Keep out of reach of children

    except under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    wash hands and rinse.

  • Inactive ingredients:

    Water, Cocamidopropyl Hydroxysultaine, Lauramidopropylamine Oxide, PEG-150 Distearate, Sodium Benzoate, Myristamidopropylamine Oxide, Lauramine Oxide, Citric Acid, Sodium Chloride, Glycerin, Fragrance, Tetrasodium EDTA, Propylene Glycol, Butylene Glycol, Ethanol, Aloe Barbadensis Leaf Juice, Dextrin, Centella Asiatica Extract, Camellia Sinensis Leaf Extract, Rosmarinus Officinalis (Rosemary) Extract, Lecithin, Phenoxyethanol, Perilla Ocymoides Leaf Extract, Ceramide NP, Beta-Sitosterol, Chlorphenesin, Potassium Sorbate, Tocopherol

  • Questions?

    USA: 1-800-253-6500

  • Package Labeling:

    Label0

  • INGREDIENTS AND APPEARANCE
    G AND H PROTECT HAND 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10056-026
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
    LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
    PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ALCOHOL (UNII: 3K9958V90M)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    ROSEMARY (UNII: IJ67X351P9)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PERILLA FRUTESCENS LEAF (UNII: T4L5881Y68)  
    CERAMIDE NP (UNII: 4370DF050B)  
    .BETA.-SITOSTEROL (UNII: S347WMO6M4)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10056-026-00250 mL in 1 BOTTLE; Type 0: Not a Combination Product04/19/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/19/2023
    Labeler - Access Business Group LLC (839830713)
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