Vaseline
FDA Label NDC 64942-0053
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 64942-0053). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - ask doctor, otc - do not use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active ingredientWHITE PETROLATUM, USP (100%)
Otc - Purpose
Purpose:Skin Protectant
Indications & Usage
Uses▪ temporarily protects and helps relieve chapped or cracked skin and lips▪ helps protect from the drying effects of wind and cold weather
Warnings
Warnings:For External Use Only
Otc - When Using
When using this product do not get into eyes
Otc - Ask Doctor
See a doctor if condition lasts more than 7 days
Otc - Do Not Use
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.
Dosage & Administration
Directions apply as needed
Inactive Ingredient
Inactive Ingredient Flavor
Otc - Questions
Questions? Call 1-800-457-7084
Package Label.Principal Display Panel
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