Purpose
Skin Protectant
Triderma Aloe Zinc Occlusive Cream
FDA Label NDC 10738-123
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Genuine Virgin Aloe Corporation for the product Triderma Aloe Zinc Occlusive (NDC 10738-123). 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 purpose, directions, inactive ingredients, warnings, active ingredient, uses, do not use:, when using this product:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Directions
Apply as soon as possible after procedure. Reapply as often as needed.
Inactive Ingredients
Aloe Barbadensis Leaf Juice*,
Avena Sativa (Oat) Kernel Flour, Cera Alba (Beeswax),
Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol, Cetyl
Alcohol, Dimethicone, Ethylhexylglycerin, Glyceryl Stearate,
Glyceryl Stearate SE, Helianthus Annuus (Sunflower) Seed
Oil, Isopropyl Palmitate, Panthenol (Pro-Vitamin B5),
Phenoxyethanol, Polysorbate 60, Potassium Cetyl
Phosphate, Propanediol, Sodium Hyaluronate, Sodium
Hydroxide, Sodium PCA, Sodium Phytate, Tocopheryl
Acetate (Vitamin E), Water (Aqua), Xanthan Gum, Zinc PCA.
*Certified Organic Ingredient - Mayacert Certifier
Warnings
For external use only
Active Ingredient
Allantoin 1.5%
Uses
temporarily protects and helps relieved chafed, chapped or cracked skin.
Do Not Use:
on deep puncture wounds, on infections, on lacerations
When Using This Product:
do not get into eyes
Keep Out Of Reach Of Children
if swallowed get medical help and contact a Poison Control Center right away.
Stop Use And Ask A Doctor If:
condition worsens or does not improve within 7 days.
Packaging
* Please review the disclaimer below.
