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OPI Personal Care Supplies Instant Foaming Hand Sanitizer Non Alcohol (OPI Correctional Industries)

Available Formats

Dosage Form Package Information Links
SOLUTION 550 mL in 1 BOTTLE (43196-514-83) Label Information
SOLUTION 3785 mL in 1 BOTTLE (43196-514-05) Label Information

Complete OPI Personal Care Supplies Instant Foaming Hand Sanitizer Non Alcohol Information

  • Drug Facts


  • Active Ingredient

    Benzalkonium Chloride 0.1%


  • Purpose

    Antimicrobial


  • Uses

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

  • Warning

    For external use only

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

    Water, dihydroxpropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance


  • Principal Display Panel

    OPI Personal Care Supplies

    Instant Foaming Hand Sanitizer Non Alcohol

    Ready-to-Use

    • Enhanced with Moisturizers
    • Kills disease causing germs within seconds
    • Effective against MRSA, VRE, E. coli (0157:H7) Staphylococcus, Streptococcus and other organisms
    • Assists with OSHA Bloodborne Pathogen Standard Compliance

    See Drug Facts panel for additional information.

    For Hospital and Professional Use Only

    Instant Foaming Hand Sanitizer Non Alcohol Label

  • INGREDIENTS AND APPEARANCE
    OPI PERSONAL CARE SUPPLIES INSTANT FOAMING HAND SANITIZER NON ALCOHOL 
    husky 514 solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:43196-514
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    benzalkonium chloride (UNII: F5UM2KM3W7) (benzalkonium - UNII:7N6JUD5X6Y) benzalkonium chloride 1 g  in 1000 mL
    Inactive Ingredients
    Ingredient Name Strength
    water (UNII: 059QF0KO0R)  
    dihydroxypropyl peg-5 linoleammonium chloride (UNII: 0Y0NQR2GH1)  
    glycereth-2 cocoate (UNII: JWM00VS7HC)  
    behentrimonium chloride (UNII: X7GNG3S47T)  
    dihydroxyethyl cocamine oxide (UNII: 8AR51R3BL5)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43196-514-05 3785 mL in 1 BOTTLE
    2 NDC:43196-514-83 550 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333 11/16/2009
    Labeler - OPI Correctional Industries (809174501)
    Establishment
    Name Address ID/FEI Business Operations
    Canberra Corporation 068080621 MANUFACTURE