Label: PETROLEUM- white petrolatum jelly

  • NDC Code(s): 41163-069-07, 41163-069-27, 41163-069-54
  • Packager: United Natural Foods, Inc. dba UNFI
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 8, 2024

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  • Active ingredients

    White petrolatum USP (100%)

  • Purpose

    Skin protectant

  • Uses

    • temporarily protects minor: -cuts -scrapes -burns
    • temporarily protects and helps relieve chapped or cracked skin and lips
    • helps protect from the drying effects of wind and cold weather
  • Warnings

    For external use only

  • Do not use on

    • deep or punture wounds
    • animal bites
    • serious burns
  • 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 within a few days
  • Keep out of reach of children

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

  • Directions

    apply as needed

  • Inactive ingredients

    None

  • Adverse Reactions

    DISTRIBUTED BY UNFI

    PROVIDENCE, RI 02908

    USA 

    855-423-2630

    *This product is not manufactured or distributed Unilever, distributor of Vaseline®.

  • Principal display panel

    EQUALINE ®

    COMPARE TO VASELINE ®*

    petroleum jelly

    white petroleum - skin protectant

    hypoallergenic

    NET WT 3.75 OZ (106 g)

    image description

  • Principal display panel

    baby basics ®

    COMPARE TO Vaseline ®*

    petroleum jelly

    white petroleum skin protectant

    hypoallergenic

    NET WT 3.75 OZ (106 g)

    image description

  • INGREDIENTS AND APPEARANCE
    PETROLEUM 
    white petrolatum jelly
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-069
    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:41163-069-27368 g in 1 JAR; Type 0: Not a Combination Product01/05/2009
    2NDC:41163-069-54106 g in 1 JAR; Type 0: Not a Combination Product01/05/2009
    3NDC:41163-069-079.9 g in 1 TUBE; Type 0: Not a Combination Product01/05/200912/31/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01601/05/2009
    Labeler - United Natural Foods, Inc. dba UNFI (943556183)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(41163-069)
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