Active Ingredient
Allantoin 0.5%
First Honey Burn Salve Cream
FDA Label NDC 81995-056
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by First Honey, Llc for the product First Honey Burn Salve (NDC 81995-056). 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, when using product, stop use and ask a doctor if, do not use on, 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
Purpose
Skin Protectant
Uses
- Temporarily protects minor
- cuts
- scrapes
- burns
- helps prevent and temporarily protects and helps relieve chafed, chapped, or cracked skin
Warnings
For external use only
When Using Product
- do not get into eyes
Stop Use And Ask A Doctor If
- Conditions worsen
- Symptoms last more than 7 days or clear up and occur again within a few days
Do Not Use On
- Deep or puncture
- wounds
- Animal bites
- Serious burns
Keep Out Of Reach Of Children.
If swallowed, get medical help, or contact a Poison Control Center right away.
Directions
- Apply as needed
Inactive Ingredients
Aloe Barbadensis Leaf Juice, Anthemis Nobilis Flower Oil, Argania Spinosa Kernel Oil, Benzyl Alcohol, Caprylic/Capric Triglyceride, Cucumis Sativus Fruit Extract, Ethylhexylglycerin, Helianthus Annuus Extract, Lavandula Angustifolia Oil, Lecithin, Manuka Honey, Mixed Tocopherols, Oryza Sativa Bran Extract, Propanediol, Rosa Canina Seed Oil, Rosmarinus Officinalis Leaf Extract, Sodium Acrylates Copolymer, Soya Bean Oil, Tetrahexyldecyl Ascorbate, Tocopherol, Water (Aqua).
Questions Or Comments?
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