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DermaCen Non-Alcohol Foaming Hand Sanitizer (Central Solutions Inc)

Available Formats

Dosage Form Package Information Links
LIQUID 1000 mL in 1 BOTTLE, PUMP (62654-141-16) Label Information
LIQUID 532 mL in 1 BOTTLE, PUMP (62654-141-14) Label Information

Complete DermaCen Non-Alcohol Foaming Hand Sanitizer Information

  • ACTIVE INGREDIENT

    Active ingredient

    Benzalkonium Chloride 0.13%


  • INDICATIONS & USAGE

    Uses

    For hand sanitizing 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 with water.

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

    Keep out of reach of children. If swallowed, call a physician or 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

    Rub hands together briskly until dry


  • INACTIVE INGREDIENT

    Inactive ingredients

    Purified Water, Glycerin, Cocamidopropyl Betaine, Triethanolamine


  • PURPOSE

    Purpose

    Hand Sanitizer


  • PRINCIPAL DISPLAY PANEL

    DermaCen

    Non-Alcohol

    Foaming Instant

    Hand Sanitizer

    For hand sanitizing

    to decrease bacteria

    on the skin

    NET CONTENTS: 18 ounces (532 mL)

    container label


  • INGREDIENTS AND APPEARANCE
    DERMACEN NON-ALCOHOL FOAMING HAND SANITIZER 
    benzalkonium chloride solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:62654-141
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride 0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:62654-141-14 532 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    2 NDC:62654-141-16 1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    3 NDC:62654-141-37 532 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 01/18/2010
    Labeler - Central Solutions Inc (007118524)
    Establishment
    Name Address ID/FEI Business Operations
    Central Solutions Inc 007118524 manufacture(62654-141)