ISO-SHIELD HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [ESC BRANDS LLC]

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ISO-SHIELD HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [ESC BRANDS LLC]
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NDC 71884-005-01
Set ID 22c7b278-87c5-4cb0-918c-4ddb70973b22
Category HUMAN OTC DRUG LABEL
Packager ESC BRANDS LLC
Generic Name
Product Class
Product Number
Application Number PART333E
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  • Drug Facts

  • Active Ingredient:

    Benzalkonium Chloride 0.13%

    Purpose:

    Antiseptic/Hand & Skin Sanitizer

  • Uses:

    Hand Sanitizer to help decrease bacteria on the skin - Recommended for repeated use

  • Warnings:

    Do not freeze, For external use only.

    Do nout use 

    in ears, eyes or mouth.

    When using this product,

    • avoid contact with the eyes, In case of contact, flush eyes with water.

    Stop use and ask a doctor

    • if redness or irritation develop and persist for more than 72 hours.

    Keep out of reach of children.

    • Children should be supervised when using this product.
  • Directions

    Apply lberally to the palms of the hands.  Rub into skin until dry.  Recocmmended for repeated use.

  • Inactive Ingredients:

    1-octadecyldimethyl (3-triethoxysilylpropyl), Ammonium Chloride, Aloe Barbadenis Leaf Extract, Aqua, C12-C15 Pareth 12, Caprylyl Glucoside, Polyhexanide, Phenoxyethanol, Triethanolamine

  • Questions?

    +1 (800) 797-1405 Mon-Fri 9:00am-5.00PM (PST)

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    ISO-SHIELD HAND SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71884-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    AMMONIUM CHLORIDE (UNII: 01Q9PC255D)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    C12-15 PARETH-12 (UNII: 131316X18L)  
    CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)  
    POLIHEXANIDE (UNII: 322U039GMF)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71884-005-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product08/14/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/14/2018
    Labeler - ESC BRANDS LLC (202621850)
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