Active Ingredient
WHITE PETROLATUM, USP (100%)
Vaseline
FDA Label NDC 64942-1869
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Conopco Inc. D/b/a Unilever for the product Vaseline (NDC 64942-1869). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredient, questions?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
skin protectant
Uses
temporarily protects minor
- cuts
- scrapes
- burns
temporarily protects and helps relieve chapped or cracked skin and lips
helps protect from the drying effects of wind and cold weather
Warnings
For external use only
When using this product do not get into eyes
See a doctor if condition last more than 7 days
Do not use on
- deep or puncture wounds
- animal bites
- serious burns
Otc - 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
apply as needed
Inactive Ingredient
Water
Questions?
Call 1-800-457-7084
Package
Vaseline Healing Jelly (Vaselinehealingjelly)
* Please review the disclaimer below.
