Petrolatum
Petrolatum is an FDA drug label for the active ingredient PETROLATUM manufactured by Greenbrier International, Inc. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20190517.
- Generic name
- PETROLATUM
- Manufacturer
- Greenbrier International, Inc.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 33992-0498
- Application
- part347
- Label effective
- 20190517
Active ingredients
Indications & Usage
Uses temporarily protects minor: cuts scrapes burns temporarily protects and helps relieve chapped or cracked skin helps protect from the drying effects of wind and cold weather
Dosage & Administration
Directions apply as needed.
Contraindications
Not available.
Warnings
Warnings For external use only. Do not use on deep puncture wounds, animal bites and serious burns. When using this product, do not get into eyes Stop use and ask doctor if condition worsens, symptoms last more than 7 days clear up and occur again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Adverse Reactions
Not available.