Label: PHARMACYS PRESCRIPTION PETROLEUM JELLY- petrolatum gel

  • NDC Code(s): 72197-044-06
  • Packager: American Consumer Products Corp
  • 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 June 15, 2021

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

  • Active Ingredients

    Active Ingredients

    White Petrolatum USP 100%

  • Inactive Ingredient

    Inactive Ingredient • Fragrance

  • Purpose

    Purpose

    Skin Protectant

  • Use

    USE: Helps treat and prevent diaper rash and seal out wetness.

  • Warnings

    Warnings: For external use only • Do not apply over deep puncture wounds, infections, or lacerations.

  • ASK DOCTOR

    If redness or swelling develops, consult a physician promptly.

  • Keep out of reach of children

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

  • Directions

    Directions: Apply liberally to clean, dry diaper area.

  • Other Information

    DISTRIBUTED BY:

    American Consumer

    Products Corp.

    Vernon, CA 90058

    Made in China

  • Package Label

    Pharmacys Prescription Petroleum Jelly

  • INGREDIENTS AND APPEARANCE
    PHARMACYS PRESCRIPTION PETROLEUM JELLY 
    petrolatum gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72197-044
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM99.9 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72197-044-06170 g in 1 JAR; Type 0: Not a Combination Product06/15/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34706/15/2021
    Labeler - American Consumer Products Corp (081101181)