Active Ingredient:
Allantoin 0.5%
Coats Aloe
FDA Label NDC 70211-705
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 70211-705). 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:, stop use if:, uses:, caution:, 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
Warnings:
For external use only.
Do not get into eyes.
Stop Use If:
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.
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.
Caution:
Do not use on deep puncture wounds, animals 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 barbadenesis leaf juice, water, butylene glycol, carbomer, triethanolamine, xanthun gum, panthenol, glycerin, chlorphenesin, potassium sorbate, sodium benzoate, beta-glucan
Questions:
Toll free 888-650-0040
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