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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            

Uses:
  • 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.

Warnings:

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

Directions:
  • 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.jpg

PETROLATUM 
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
PETROLATUM (PETROLATUM) PETROLATUM1 g  in 1 g
Packaging
#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)
Establishment
NameAddressID/FEIOperations
Choice Laboratories650070394manufacture(67777-211)
Establishment
NameAddressID/FEIOperations
Jell Pharmaceuticals Pvt. Ltd.726025211manufacture(67777-211)

 
Dynarex Corporation

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Medically reviewed on Apr 9, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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