Label: MEDPRIDE- white petrolatum ointment

  • NDC Code(s): 52410-3020-2, 52410-3020-3, 52410-3020-4, 52410-3020-5
  • Packager: Shield Line LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 20, 2024

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  • Active Ingredient

    White Petroleum Jelly USP [100% w/w]

  • Purpose

    Skin Protectant

  • Uses

    ■ helps treat and prevent diaper rash ■ helps seal out wetness ■ temporarily protects minor ■ cuts ■ scrapes ■ burns ■ temporarily helps protect and relieve chapped and cracked skin or lips ■ helps prevent and protect chafed skin or minor skin irritations associated with diaper rash ■ with each diaper change, espicially at bedtime when exposure to wet diapers may be prolonged

  • Warnings

    For external use only

  • When using this product

    ■ do not get into eyes

  • Stop use and ask a doctor if

    ■ condition worsens ■ symptoms last more than 7 days or clear up and occur again in a few days

  • Do not use on

    ■ deep puncture woulnd ■ animal bites ■ serious burns

  • 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

    ■ change wet and soiled diapers promptly ■ cleanse the diaper area and allow to dry ■ apply as needed

  • Other Information

    ■ store at 59-86F (15-30C) ■ avoid excessive heat

  • Inactive Ingredient

    None

  • Package Label

    Principal Display and Drug Fact Panel

  • INGREDIENTS AND APPEARANCE
    MEDPRIDE 
    white petrolatum ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52410-3020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM100 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52410-3020-25 g in 1 PACKET; Type 0: Not a Combination Product09/23/2013
    2NDC:52410-3020-357 g in 1 TUBE; Type 0: Not a Combination Product09/23/2013
    3NDC:52410-3020-4113 g in 1 TUBE; Type 0: Not a Combination Product09/23/2013
    4NDC:52410-3020-5425 g in 1 JAR; Type 0: Not a Combination Product09/23/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01609/23/2013
    Labeler - Shield Line LLC (078518916)
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