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Capent (Laboratorios Columbia S.A. de C.V.)

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OINTMENT 42.5 g in 1 TUBE (59567-001-42) Label Information

Complete Capent Information

  • ACTIVE INGREDIENT

    Active Ingredients

    Zinc Oxide 25%

    Lanolin 15.5%


  • PURPOSE

    Purpose

    Skin protectant

    Skin protectant


  • INDICATIONS & USAGE

    Uses ● Helps treat and prevent diaper rash ●Protects minor skin irritation associated with diaper rash ● Helps protect from wetness


  • WARNINGS

    Warnings For external use only


  • WHEN USING

    When using this product ● Do not get into eyes


  • STOP USE

    Stop use and ask a doctor if ● Condition worsens ● Symptoms last for more than 7 days or clear up and occur within a few days


  • 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 ● Change wet or soiled diapers promptly ● Cleanse the diaper area and allow to dry ● Apply ointment liberally as often as necessary with each diaper change, especially at bedtime or any time prolonged exposure to wet diaper is expected


  • SPL UNCLASSIFIED SECTION

    Other information ● store away from heat ● do not use if carton is broken ● see bottom of box and tube for lot number and expiration date


  • INACTIVE INGREDIENT

    Inactive ingredients: allantoin, benzalkonium chloride, BHA, cod liver oil, fragrance, glyceryl monostearate, mineral oil, paraffin, propyl gallate, talc


  • INGREDIENTS AND APPEARANCE
    CAPENT  DIAPER RASH
    zinc oxide lanolin ointment
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:59567-001
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 25 g  in 100 g
    LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H) LANOLIN 15.5 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    ALLANTOIN (UNII: 344S277G0Z)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)  
    COD LIVER OIL (UNII: BBL281NWFG)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PROPYL GALLATE (UNII: 8D4SNN7V92)  
    TALC (UNII: 7SEV7J4R1U)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:59567-001-42 42.5 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part347 03/01/2013
    Labeler - Laboratorios Columbia S.A. de C.V. (812685253)
    Establishment
    Name Address ID/FEI Business Operations
    Laboratorios Columbia S.A. de C.V. 812685253 manufacture(59567-001)