Active Ingredient
White Petrolatum(40%)
Flanders Healing
FDA Label NDC 54323-103
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Flanders Inc for the product Flanders Healing (NDC 54323-103). 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, uses:, do not use on, when using this product:, stop and ask a doctor if:, keep out of reach of children, if pregnant or breast-feeding, directions:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses:
- Temporarily protects minor: Cuts, scrapes and burns
- Temporarily protects chapped or cracked skin.
- Helps protect from the drying effects of wind and cold weather.
Do Not Use On
- Deep or puncture wounds
- animal bites
- serious burns
When Using This Product:
Do not get into eyes
Stop And Ask A Doctor If:
- Condition worsens
- Symptoms last more than 7 days or 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.
If Pregnant Or Breast-Feeding
Ask a health care professional before use.
Directions:
- Apply as needed
Inactive Ingredients:
Aloe extract, Beeswax, Helianthus Annus (sunflower oil), Olea Europea (olive oil), Tocopheryl acetate (Vitamin E)
Questions?
855-649-7274
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