Label: TECHNI-PRO FOAMING HAND SANITIZER- benzalkonium chloride liquid

  • NDC Code(s): 59555-403-11, 59555-403-12
  • Packager: R & R Lotion, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 March 15, 2022

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Benzalkonium Chloride 0.1%

  • Purpose

    Antimicrobial

  • Uses

    • For hand sanitizing to decrease bacteria on the skin
    • Recommended for repeated use
  • Warnings

    For external use only

    When using this product avoid contact with eyes. If contact with eyes, flush with water.

    Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Pump a small amount of foam into palm of hand
    • Rub thoroughly over all surfaces of both hands
    • Rub hands together briskly until dry.
  • Inactive Ingredients

    DI Water, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Glycereth-2 Ocoate, Behentrimonium Chloride, Dihydroxyethyl Cocamine Oxide

  • PRINCIPAL DISPLAY PANEL - 3785 mL Bottle Label

    TECHNI-PRO

    FOAMING
    HAND SANITIZER

    TestEquity Part #:
    TNP-ICHS-GAL

    PACKAGING SIZE: 128oz.

    PRINCIPAL DISPLAY PANEL - 3785 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    TECHNI-PRO FOAMING HAND SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59555-403
    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)  
    Cetrimonium Chloride (UNII: UC9PE95IBP)  
    Laurtrimonium Chloride (UNII: A81MSI0FIC)  
    Dihydroxyethyl Cocamine Oxide (UNII: 8AR51R3BL5)  
    Glycereth-17 Cocoate (UNII: 3057VPT0KC)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59555-403-12591 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/10/2022
    2NDC:59555-403-113785 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product03/10/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333A03/10/2022
    Labeler - R & R Lotion, Inc (062979000)
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