Label: PETROLEUM- white petrolatum jelly

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 11, 2019

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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

  • When using this product

    • do not get into eyes
  • Stop use and ask a doctor

    if condition worsens or does not improve within 7 days

  • Do not use on

    • deep or puncture wounds
    • animal bites
    • serious burns
  • Keep out of reach of children

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

  • Directions

    Apply as needed

  • Disclaimer

    This product is not manufactured or distributed by Unilever, distributor of Vaseline 

  • Adverse reaction

    Distributed by:

    Geiss, Destin and Dunn, Inc

    Peachtree City, GA 30269

    www. valuelabels.com

    1-866-696-0957

    069.001/069AA

  • principal display panel

    GoodSense

    Petroleum

    Jelly

    Skin Protectat

    White Petrolatum USP

    100%

    SATISFACTION 

    GUARENTEED

    NET WT 13 OZ (368 g)

    069.001/069AA

    image description

  • INGREDIENTS AND APPEARANCE
    PETROLEUM 
    white petrolatum jelly
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50804-069
    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:50804-069-27368 g in 1 JAR; Type 0: Not a Combination Product06/15/1992
    2NDC:50804-069-54106 g in 1 JAR; Type 0: Not a Combination Product06/15/1992
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34706/15/1992
    Labeler - Geiss, Destin and Dunn, Inc (076059836)
    Registrant - Vi-Jon (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon088520668manufacture(50804-069)
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