Label: TINCTURE MERTHIOLATE- benzalkonium chloride tincture

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2023

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  • Active Ingredient

    Benzalkonium chloride 0.13%

    Purpose

    First Aid Antiseptic

  • Uses

    First aid antiseptic to help prevent infection in minor:

    cuts - scrapes - burns

  • Warnings

    For external use only.

    Flammable. Keep away from sparks, heat and fire.

    Consult a doctor before use if you have - deep or puncture wounds - animal bites - serious burns

    When using this product

    • do not use in or near the eyes
    • do not apply in large quantities or over large areas of the body
    • do not apply over raw surtaces or blistered areas
    • do not use longer than 1 week unless directed by a doctor

    Stop use and consult a doctor if

    • the condition persists or gets worse

    Keep out of reach of children.

    II swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    • adults and children 2 years of age and older: clean the affected area
    • apply a small amount of this product to the area 1 to 3 times daily _ may be covered with a sterile bandage. If bandaged, let dry first
    • children under 2 years of age: ask a doctor
  • Other Information

    • will stain skin and clothing
  • Inactive Ingredients

    acetone, alcohol, DandC red no. 22, purified water

  • Product Labeling

    De La Cruz Merthiolate

    Tincture Merthiolate

    48% Alcohol

    Mercury Free

    First Aid Antiseptic

    For External Use Only

    1 FL OZ (30 mL)

    Distributed by

    De La Cruz Products

    A Division of DLC Laboratories, Inc.

    Paramount, CA 90723 USA

    Questions: 1-800-858-3889

    www.dlclabs.com

    Warnings: FLAMMABLE, KEEP AWAY FROM SPARKS, HEAT AND FIRE.

  • INGREDIENTS AND APPEARANCE
    TINCTURE MERTHIOLATE 
    benzalkonium chloride tincture
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1532
    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
    ACETONE (UNII: 1364PS73AF)  
    ALCOHOL (UNII: 3K9958V90M)  
    D&C RED NO. 22 (UNII: 1678RKX8RT)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24286-1532-730 mL in 1 BOTTLE; Type 0: Not a Combination Product12/13/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/22/2013
    Labeler - DLC Laboratories, Inc (093351930)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114analysis(24286-1532) , manufacture(24286-1532) , pack(24286-1532) , label(24286-1532)
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