FDA Label for Triderma Foot Defense
View Indications, Usage & Precautions
Triderma Foot Defense Product Label
The following document was submitted to the FDA by the labeler of this product Genuine Virgin Aloe Corporation. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Allantoin 1.5%
Otc - Purpose
Skin Protectant
Indications & Usage
Helps prevent and temporarily protects and helps relieve chafed, chapped or cracked skin.
Warnings
For external use only.
Otc - Do Not Use
- on deep puncture wounds
- on infections
- on lacerations
Otc - When Using
do not get into eyes
Otc - Stop Use
stop use and ask a doctor if conditin worsens or does not improve within 7 days.
Otc - Keep Out Of Reach Of Children
if swallowed get medical help and contact a poison control center right away.
Dosage & Administration
Apply twice a day or as often as needed.
Storage And Handling
- Do not use if the tube seal is broken
- Store at room temperatue
Otc - Questions
Questions: 1-800-279-7282 M-F 8 am - 4 pm PST
Inactive Ingredient
Aloe Barbadensis (Aloe Vera) Leaf Juice*, Avena Sativa (Oat) Kernel Flour, Butyrospermum Parkii (Shea) Butter, Cera Alba (Beeswax), Cetearyl Alcohol, Cetyl Alcohol, Dimethicone, Ethylhexylglycerin, Isopropyl Palmitate, Lactic Acid, Panthenol (Pro-Vitamin B5), Phenoxyethanol, Polysorbate 60, Sodium Hyaluronate, Sodium Hydroxide, Sodium PCA, Sodium Phytate, Tocopheryl Acetate (Vitamin E), Urea, Water, Zinc PCA.
*Certified Organic Ingredient - Mayacert Certifier
* Please review the disclaimer below.
