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PETROLATUM by Dynarex Corporation

Dosage form: jelly
Ingredients: PETROLATUM 1g in 1g
Labeler: Dynarex Corporation
NDC Code: 67777-211

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.

White Petrolatum

Active Ingredient                            Purpose

White Petrolatum 100%                 Skin Protectant            

  • Helps treat and prevent diaper rash
  • Helps seal out wetness
  • Temporarily protects minor * cuts * scrapes * burns
  • Temporarily helps protect and helps relieve chapped and cracked skin and lips
  • Helps prevent and protect from the drying effects of wind and cold weather
  • Helps prevent and protect chaffed skin or minor skin irritations associated with diaper rash
  • With each diaper change, especially at bed time when exposure to wet diapers may be prolonged.


For external use only.

When using this product:

Do not get in eyes.

Stop use and ask a doctor if:
  • Condition worsens
  • symptoms last more than 7 days or clear up and occur in 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

  • Change wet and soiled diapers promptly
  • cleanse the diaper area and allow to dry
  • apply as needed

Other information:
  • Store at room temperature 15 Deg C - 30 Deg C (59 Deg F - 86 Deg F)
  • Avoid excessive heat 

Principal Display Panel


petrolatum jelly
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-211
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
#Item CodePackage Description
1NDC:67777-211-01144 PACKET (PACKET) in 1 BOX
15 g in 1 PACKET
2NDC:67777-211-02425.2 g in 1 JAR
3NDC:67777-211-031 TUBE (TUBE) in 1 BOX
328.35 g in 1 TUBE
4NDC:67777-211-076 TUBE (TUBE) in 1 BOX
4113.4 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34701/31/2010
Labeler - Dynarex Corporation (008124539)
Registrant - Dynarex Corporation (008124539)
Choice Laboratories650070394manufacture(67777-211)
Jell Pharmaceuticals Pvt. Ltd.726025211manufacture(67777-211)

Revised: 04/2013
Dynarex Corporation

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.