Label: SKIN PROTECTANT- petrolatum ointment

  • NDC Code(s): 11344-247-17
  • Packager: Consumer Product Partners, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 28, 2024

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

View All Sections
  • Active ingredient

    Petrolaturm 41%

  • Purpose

    Skin protectant (ointment)

  • Uses

    • temporarily protects minor: cuts, scrapes, burns
    • temporarily protects and helps relieve chapped and 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 in eyes
  • Stop use

    • 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 contract a Poison Control Center right away

  • Directions

    • apply as needed
  • Inactive ingredients

    minerol oil, ceresin, lanolin alcohol, panthenol, glycerin, bisabolol

  • Disclaimer

    *This product is not manufactured or distributed by Beiersdorf Inc., distributor Aquaphor ®Healing Ointment.

  • Adverse reactions

    Distributed by: Vi-Jon, Inc.

    8515 Page Ave.

    St. Louis, MO, 63114

  • Principal display panel

    SWAN ®

    ADVANCED HEALING OINTMENT

    skin protectant

    • Fragrance free
    • For dry, cracked or irritated skin
    • Soothes and protects

    Compare to Aquaphor ®Healing Ointment*

    NET WT 1.75 OZ (50 g)

    image description

  • INGREDIENTS AND APPEARANCE
    SKIN PROTECTANT 
    petrolatum ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-247
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM410 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    MINERAL OIL (UNII: T5L8T28FGP)  
    CERESIN (UNII: Q1LS2UJO3A)  
    LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11344-247-1750 g in 1 TUBE; Type 0: Not a Combination Product02/28/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01602/28/2024
    Labeler - Consumer Product Partners, LLC (119091520)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(11344-247)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!