Active Ingredient
Allantoin 0.5%
Coats Aloe
FDA Label NDC 58826-705
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tychasis Corporation for the product Coats Aloe (NDC 58826-705). 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, warnings, uses:, otc - stop use, inactive ingredients, directions, use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Skin protectant.
Warnings
For external use only.
When using this product do not get into eyes.
Uses:
Temporarily protects minor
- cuts
- scrapes
- burns
Helps prevent and temporarily protects and helps relieve chaffed, chapped or cracked skin.
Helps prevent and protect from the drying effects of wind and cold weather.
Otc - Stop Use
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.
Inactive Ingredients
aloe barbadenesis leaf juice, water, butylene glycol, carbomer, triethanolamine, xanthum gum, panthenol, glycerin, chlorphensin, potassium sorbate, sodium benzoate, beta-glucan
Directions
Apply as needed
Use
Apply as needed
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.
Otc - Do Not Use
Do not use on deep puncture wounds, animal bits, serious burns.
* Please review the disclaimer below.
