Vaseline
FDA Label NDC 64942-0034

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 64942-0034). 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

Otc - Active Ingredient

Active ingredientWHITE PETROLATUM, USP (100%)

Otc - Purpose

PurposeSkin Protectant

Indications & Usage

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

WarningsFor 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

Otc - Questions

Questions?  Contact the Consumer Information Center 1-800-457-7084

Package Label.Principal Display Panel

VPJ 13 oz. PDP

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