Label: WALGREENS HEALING PETROLATUM SKIN PROTECTANT- 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 April 20, 2023

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  • Active ingredient

    Petrolatum 46.5%

  • Purpose

    Skin protectant

  • Uses

    • temporarily protects and helps relieve chapped or cracked skin and lips
    • temporarily protects minor:

    • cuts

    • scrapes

    • burns

    • 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 • symptoms last more than 7 days or clear up and occur again within a few 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.

  • Other information

    • may stain some fabrics
  • Inactive Ingredients

    Mineral Oil, Paraffin, Ozokerite, Dimethicone, Hyaluronic Acid, Sodium Hydroxide, Ceramide 1, Ceramide 3, Ceramide 6-II, Tocopheryl Acetate, Phytosphingosine, Cholesterol, Sodium Lauroyl Lactylate, Carbomer, Panthenol, Water, L-Proline, Xanthan Gum.

  • Label

    W41283A1

  • INGREDIENTS AND APPEARANCE
    WALGREENS HEALING PETROLATUM SKIN PROTECTANT 
    petrolatum ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0182
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM465 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROLINE (UNII: 9DLQ4CIU6V)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)  
    WATER (UNII: 059QF0KO0R)  
    HEXAMETHYLDISILOXANE (UNII: D7M4659BPU)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CERAMIDE NP (UNII: 4370DF050B)  
    CHOLESTEROL (UNII: 97C5T2UQ7J)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)  
    CERAMIDE AP (UNII: F1X8L2B00J)  
    CERESIN (UNII: Q1LS2UJO3A)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-0182-0989 mL in 1 TUBE; Type 0: Not a Combination Product07/02/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM01607/02/2019
    Labeler - WALGREEN COMPANY (008965063)
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