Label: PETROLEUM JELLY- white petrolatum ointment

  • NDC Code(s): 20276-505-11, 20276-505-12, 20276-505-13, 20276-505-14, view more
    20276-505-15, 20276-505-16, 20276-505-17, 20276-505-18, 20276-505-19, 20276-505-20
  • Packager: Delta Brands Inc.
  • 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 February 8, 2022

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

View All Sections
  • Active Ingredient

    White Petrolatum USP (100%)

  • Purpose

    Skin protectant

  • Uses

    • For the temporary protection of minor cuts, scrapes, burns  and sunburn.
    • Helps to temporarily protect chafed, chapped, cracked or windburned skin and lips.
  • Warnings

    For External Use Only 

  • Do not use

    over deep or puncture wounds infections or lacerations. Ask a doctor

  • When using this product

    avoid contact with eyes

  • Stop use and ask a doctor

    if condition worsens or does not improve within 7 days

  • Keep out of reach of children

    if swallowed get medical help or contact a Poison Control Center right away.

  • Directions

    Apply product liberally as often as necessary

  • Inactive ingredient

  • Package Label

    image of package label

  • INGREDIENTS AND APPEARANCE
    PETROLEUM JELLY 
    white petrolatum ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:20276-505
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM1 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:20276-505-11100 g in 1 JAR; Type 0: Not a Combination Product05/30/2011
    2NDC:20276-505-12113 g in 1 JAR; Type 0: Not a Combination Product05/30/2011
    3NDC:20276-505-13142 g in 1 JAR; Type 0: Not a Combination Product05/30/2011
    4NDC:20276-505-14170 g in 1 JAR; Type 0: Not a Combination Product05/30/2011
    5NDC:20276-505-15198 g in 1 JAR; Type 0: Not a Combination Product05/30/2011
    6NDC:20276-505-16226 g in 1 JAR; Type 0: Not a Combination Product05/30/2011
    7NDC:20276-505-17255 g in 1 JAR; Type 0: Not a Combination Product05/30/2011
    8NDC:20276-505-18283 g in 1 JAR; Type 0: Not a Combination Product05/30/2011
    9NDC:20276-505-19368 g in 1 JAR; Type 0: Not a Combination Product05/02/2016
    10NDC:20276-505-20150 g in 1 JAR; Type 0: Not a Combination Product02/03/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34705/30/2011
    Labeler - Delta Brands Inc. (102672008)
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!