Label: VASELINE LIP THERAPY ADVANCED FORMULA- petrolatum ointment 

  • NDC Code(s): 64942-0053-1, 64942-0053-2
  • Packager: Conopco Inc. d/b/a Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 10/12

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  • ACTIVE INGREDIENT

    Active ingredient
    WHITE PETROLATUM, USP (100%)
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  • PURPOSE

    Purpose:
    Skin Protectant
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  • INDICATIONS & USAGE

    Uses
      temporarily protects and helps relieve chapped or cracked skin and lips
      helps protect from the drying effects of wind and cold weather
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  • WARNINGS

    Warnings:
    For External Use Only

    When using this product do not get into eyes

    See a doctor if condition lasts more than 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.
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  • DOSAGE & ADMINISTRATION

    Directions apply as needed Close
  • INACTIVE INGREDIENT

    Inactive Ingredient  Flavor Close
  • QUESTIONS

    Questions?  Call 1-800-457-7084 Close
  • PRINCIPAL DISPLAY PANEL

    VLT 0.35 oz. PDPVaseline Lip Therapy Advanced 0.35 oz PDP

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  • PRINCIPAL DISPLAY PANEL

    VLT blister cardVaseline Lip Therapy Advanced 0.35 oz blister card

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  • INGREDIENTS AND APPEARANCE
    VASELINE  LIP THERAPY ADVANCED FORMULA
    petrolatum ointment
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:64942-0053
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    petrolatum (petrolatum) petrolatum 100 g  in 100 g
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:64942-0053-2 1 in 1 BLISTER PACK
    1 NDC:64942-0053-1 10 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part347 01/20/2004
    Labeler - Conopco Inc. d/b/a Unilever (001375088)
    Establishment
    Name Address ID/FEI Business Operations
    Conopco Inc. d/b/a Unilever 198786444 manufacture(64942-0053)
    Establishment
    Name Address ID/FEI Business Operations
    Alberto-Culver USA Inc. 021679448 manufacture(64942-0053)
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