Label: SKIN-LUBE- petrolatum, dimethicone ointment

  • NDC Code(s): 82345-860-01, 82345-860-02, 82345-860-05, 82345-860-25
  • Packager: The Hygenic Company, LLC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 5, 2023

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

View All Sections
  • Drug Facts

  • Active Ingredients

    Petrolatum 85%

    Dimethicone 1.5%

    Purpose

    Skin Protectant

  • Uses

    Temporarily protects minor • cuts • scrapes • burns – Helps prevent, temporarily protects, and helps relieve chafed, chapped or cracked skin. Helps prevent and protect from the drying effects of wind and cold weather.

  • Warnings

    For external use only.

    Do not use on

    • deep or puncture wounds • animal bites • serious burns

    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.

    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

    – Store in a cool dry place with lid closed tightly.

  • Inactive Ingredients

    – Diazolidinyl Urea, Methylparaben, Propylene Glycol, Propylparaben, Zinc Stearate

  • Questions?

    (800) 345-2231

  • Package Labeling:82345-860-25

    Label2

  • Package Labeling:82345-860-05

    Label3

  • Package Labeling:82345-860-01

    Label4

  • Package Labeling:82345-860-02

    Label5

  • INGREDIENTS AND APPEARANCE
    SKIN-LUBE 
    petrolatum, dimethicone ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82345-860
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM850 mg  in 1 g
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE15 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    ZINC STEARATE (UNII: H92E6QA4FV)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82345-860-251134 g in 1 BOTTLE; Type 0: Not a Combination Product04/01/2022
    2NDC:82345-860-052270 g in 1 BOTTLE; Type 0: Not a Combination Product04/01/2022
    3NDC:82345-860-01454 g in 1 BOTTLE; Type 0: Not a Combination Product04/01/2022
    4NDC:82345-860-0278 g in 1 JAR; Type 0: Not a Combination Product04/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01604/01/2022
    Labeler - The Hygenic Company, LLC. (004163390)
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!