Label: VASELINE LIP THERAPY CHERRY- petrolatum ointment

  • 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 October 2, 2012

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

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

    Purpose:
    Skin Protectant
  • 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
  • WARNINGS

    Warnings
    For External Use Only

    When using this product do not get in eyes

    See a doctor if condition lasts more than 7 days

    Do not use on ▪deep or puncture woundsanimal bitesserious burns

    Keep out of reach of children.  If swallowed get medical help or contact a Poison Control Center right away.
  • DOSAGE & ADMINISTRATION

    Directions apply as needed
  • INACTIVE INGREDIENT

    Inactive Ingredient  Flavor, Sodium Saccharin
  • QUESTIONS

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

    VLT Cherry 0.35 oz. PDPVaseline Lip Therapy Cherry 0.35 oz PDP

  • PRINCIPAL DISPLAY PANEL

    VLT Cherry Blister CardVaseline Lip Therapy Cherry 0.35 oz blister card

  • INGREDIENTS AND APPEARANCE
    VASELINE  LIP THERAPY CHERRY
    petrolatum ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-0054
    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
    SACCHARIN SODIUM DIHYDRATE (UNII: SB8ZUX40TY)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-0054-21 in 1 BLISTER PACK
    1NDC:64942-0054-110 g in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34701/20/2004
    Labeler - Conopco Inc. d/b/a Unilever (001375088)
    Establishment
    NameAddressID/FEIBusiness Operations
    Conopco Inc. d/b/a Unilever198786444manufacture(64942-0054)
    Establishment
    NameAddressID/FEIBusiness Operations
    Alberto-Culver USA Inc.021679448manufacture(64942-0054)