Home > Drugs A-Z > De La Cruz Mercurochrome

De La Cruz Mercurochrome (DLC Laboratories, Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 30 mL in 1 BOTTLE (24286-1553-1) Label Information

Complete De La Cruz Mercurochrome Information

  • Active Ingredients

    Benzalkonium Chloride 0.13%

    Liddocaine Hydrochloride 2.5%


  • Purpose

    First Aid Antiseptic

    Pain Reliever


  • Uses

    first aid to help prevent bacterial contamination or skin infection and temporarily relieves pain and itching associated with cuts, scrapes, burns, sunburn, skin irritations


  • Warnings

    For external use only.

    Ask a dotor 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 over large ares of the body or in large quantities. do not apply over raw surfaces or blistered areas.

    Stop use and ask a doctor if

    condition worsens, symptoms persist for more than 7 days, or clear up and occur again with in a few days.

    Keep out of the reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.


  • Directions

    adults and children 2 years of age and older: clean the affected area; apply a small amount of this product on the area 1 to 3 times daily; may be covered with a sterile bandage (let dry first). children unde4r 2 years, ask a doctor


  • Other Information

    protect from excessive heat



  • Inactive Ingredients

    acetone, purified water USP


  • PRINCIPAL DISPLAY PANEL

    De La Cruz

    Mercurochrome

    (Benzalkonium Chloride and Lidocaine hydrochloride)


    Helps prevent skin infection and relieves pain and itching in minor cuts, scrapes, burns and insect bites.
    FIRST AID ANTISEPTIC AND PAIN RELIEVER

    Mercury Free
    Contents 1fl oz (30mL)

    Manufactured by
    DLC Laboratories, Inc.
    PARAMOUNT, CA  90723 USA

    1-800-858-3889 / www.dlclabs.com


  • INGREDIENTS AND APPEARANCE
    DE LA CRUZ MERCUROCHROME 
    benzalkonium chloride and lidocaine hydrochloride liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:24286-1553
    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 mL  in 100 mL
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 2.5 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    ACETONE (UNII: 1364PS73AF)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:24286-1553-1 30 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 06/30/2011
    Labeler - DLC Laboratories, Inc. (093351930)
    Registrant - DLC Laboratories, Inc. (093351930)
    Establishment
    Name Address ID/FEI Business Operations
    DLC Laboratories, Inc. 093351930 manufacture