Label: UNIVERSAL PURE PETROLEUM- white petroleum jelly

  • NDC Code(s): 52000-005-19, 52000-005-20, 52000-005-21, 52000-005-22, view more
    52000-005-23, 52000-005-24, 52000-005-25, 52000-005-26, 52000-005-27, 52000-005-28
  • Packager: Universal Distribution Center LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 17, 2024

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  • ACTIVE INGREDIENT

    Active ingredient

    White Petrolatum USP (100 %)

  • PURPOSE

    Purpose

    Skin Protectant

  • INDICATIONS & USAGE

    Uses

    • For the temporary protection of minor cuts, scrapes, burns and sunburn.
    • Helps to temporarily protect chafed, chapped, cracked or windburned skin and lips.
  • WARNINGS

    Warnings

    For External Use Only.

    Do not use over deep or puncture wounds, infections or lacerations. Ask a doctor.

    When using this product avoid contact with eyes.

    Stop use and ask doctor if condition worsens or does not improve within 7 days.

    Keep out of reach of children if swallowed get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions

    Apply product as liberally, as often as necessary.

  • INACTIVE INGREDIENT

    Inactive ingredients

    None

  • SPL UNCLASSIFIED SECTION

    PRINCIPAL DISPLAY PANEL

    UNIVERSAL PURE PETROLEUM JELLY
    SKIN PROTECTANT
    NET WT. 13 OZ (368 g)

  • PRINCIPAL DISPLAY PANEL

    PRINCIPAL DISPLAY PANEL 100% PURE PETROLEUM JELLY Net Wt. 8 fl. oz. (250g) 8 onzas

  • INGREDIENTS AND APPEARANCE
    UNIVERSAL PURE PETROLEUM 
    white petroleum jelly
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM1 g  in 1 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52000-005-19226 g in 1 JAR; Type 0: Not a Combination Product11/07/2022
    2NDC:52000-005-2045 g in 1 JAR; Type 0: Not a Combination Product11/07/2022
    3NDC:52000-005-21100 g in 1 JAR; Type 0: Not a Combination Product11/07/2022
    4NDC:52000-005-22113 g in 1 JAR; Type 0: Not a Combination Product11/07/2022
    5NDC:52000-005-23170 g in 1 JAR; Type 0: Not a Combination Product11/07/2022
    6NDC:52000-005-24198 g in 1 JAR; Type 0: Not a Combination Product11/07/2022
    7NDC:52000-005-25283 g in 1 JAR; Type 0: Not a Combination Product11/07/2022
    8NDC:52000-005-26368 g in 1 JAR; Type 0: Not a Combination Product11/07/2022
    9NDC:52000-005-27450 g in 1 JAR; Type 0: Not a Combination Product11/07/2022
    10NDC:52000-005-28500 g in 1 JAR; Type 0: Not a Combination Product11/07/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01602/06/2013
    Labeler - Universal Distribution Center LLC (019180459)
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