Label: PROCURE- zinc oxide ointment

  • NDC Code(s): 55681-304-03, 55681-304-04, 55681-304-05
  • Packager: TWIN MED, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 8, 2024

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  • Active Ingredient

    Zinc Oxide 20% w/w

  • Purpose

    Skin Protectant

  • Uses

    ■ helps treat and prevent diaper rash ■ dries the oozing and weeping of ■ poison ivy ■ poison oak ■ poison sumac

  • Warnings

    For external use only

  • When using this product

    ■ do not get into eyes

    ■ do not use over large areas of the body

  • Stop use and ask a doctor if

    ■ the condition worsens ■ symptoms last more than 7 days or clear up and occur again in a few days ■ if you are allergic to any of these ingredients

  • 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

  • Directions

    ■ for diaper rash ■ change wet and soiled diapers promptly ■ cleanse the diaper area and allow to dry ■ apply ointment liberally with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged ■ for poison ivy, oak sumac ■ apply ointment liberally as often as needed

  • Other Information

    ■ store at 59-86F (15-30C)

  • Inactive Ingredients

    cetostearyl alcohol, cetomacrogol 1000, lanolin, light liquid paraffin, white soft parrafin

  • Package Label

    Principal Display and Drug Fact Panel

  • INGREDIENTS AND APPEARANCE
    PROCURE 
    zinc oxide ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55681-304
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE20 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    LANOLIN (UNII: 7EV65EAW6H)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETETH-20 (UNII: I835H2IHHX)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55681-304-0328.3 g in 1 TUBE; Type 0: Not a Combination Product05/23/2013
    2NDC:55681-304-0456.6 g in 1 TUBE; Type 0: Not a Combination Product05/23/2013
    3NDC:55681-304-05425 g in 1 JAR; Type 0: Not a Combination Product05/23/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01605/23/2013
    Labeler - TWIN MED, LLC (009579330)
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