SANISMART 2 (BENZALKONIUM CHLORIDE) LIQUID [REGISTERED CHEMICALS CORPORATION]

SANISMART 2 (BENZALKONIUM CHLORIDE) LIQUID [REGISTERED CHEMICALS CORPORATION]
PDF | XML

NDC 72130-002-01, 72130-002-02
Set ID eb1d4d76-c2df-475a-98bb-541a5ea75769
Category HUMAN OTC DRUG LABEL
Packager Registered Chemicals Corporation
Generic Name
Product Class
Product Number
Application Number PART333A
  • ACTIVE INGREDIENT

    Active ingredient

    Benzalkonium Chloride 0.13%

  • PURPOSE

    Purpose

    Antimicrobial

  • INDICATIONS & USAGE

    Uses   •For hand washing to decrease bacteria on the skin

             •Recommended for repeated use

  • WARNINGS

    Warnings

    For external use only.

    When using this product avoid contact with eyes. In case of eye contact, flush eyes

    thoroughly with water.

    Stop use and ask a doctor if irritation or redness develop, or if condition persists for more

    than 72 hours.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a

    Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions   •Pump a small amount of foam into palm of hand.

    •Rub thoroughly over all surfaces of both hands for 15 seconds.   •Rinse with potable water.

  • INACTIVE INGREDIENT

    Inactive ingredients  Water (Aqua), coco-glucoside, laurtrimonium chloride,

    coamidopropylamine oxide, citric acid

  • QUESTIONS

    Questions or comments? 781-803-7800   •info@registeredchemicals.com

  • PRINCIPAL DISPLAY PANEL

    image description

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    SANISMART 2 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72130-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72130-002-021250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/01/2018
    2NDC:72130-002-013785 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/01/2018
    Labeler - Registered Chemicals Corporation (046652831)

Related Drugs