Warnings
For external use only
Triderma Stubborn Eczema Itch Relief Cream
FDA Label NDC 10738-169
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 Stubborn Eczema Itch Relief (NDC 10738-169). 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 warnings, purpose, directions, inactive ingredients, 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
Purpose
Skin Protectant
Directions
apply twice a day or as often as needed.
Inactive Ingredients
Allantoin, Aloe Barbadensis Leaf Juice*, Arnica Montana Flower Extract, Avena Sativa Kernel Oil, Butyrospermum Parkii (Shea) Butter, Cera Alba (Beeswax), Cetearyl Alcohol, Cetyl Alcohol, Dimethicone, Ethylhexylglycerin, Glycerin, Isopropyl Palmitate, Lactic Acid, Panthenol (Pro-Vitamin B5), Phenoxyethanol, Polysorbate 60, Sodium Hyaluronate, Sodium PCA, Sodium Phytate, Tocopheryl Acetate (Vitamin E), Urea, Water, Zinc PCA
*Certified Organic Ingredient - Mayacert Certifier
Active Ingredient
Colloidal Oatmeal 2%
Uses
temporarily protects and helps relieve minor skin irritation and itching due to: •eczema •rashes
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.
