Active Ingredient
Petrolatum 44.28%
Aquagard
FDA Label NDC 67777-146
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dynarex Corporation for the product Aquagard (NDC 67777-146). 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, stop use and ask a doctor if, do not use, otc - keep out of reach of children, directions, 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 dry, chapped, or cracked skin and lips
- Helps protect skin from the drying effects of wind and cold weather
Warnings
For External Use Only
Avoid contact with eyes. In case of contact, flush thoroughly with water.
Stop Use And Ask A Doctor If
- condition worsens
- symptoms last more than 7 days or clear up and occur again within a few days
Do Not Use
on deep puncture wounds, animal bites, or serious burns.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Apply as needed or as directed by a physician.
Other Information
Store at room temperature (59° - 86°F)
Inactive Ingredients
Ceresin Wax, Dexpanthenol, Glycerin, Lanolin Alcohol, Mineral Oil
Questions?
1-888-DYNAREX Monday-Friday, 9AM-5PM EST
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