Otc - Active Ingredient
Benzethonium Chloride 0.12%
Triderma Pressure Sore Relief Liquid
FDA Label NDC 10738-031
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 Pressure Sore Relief (NDC 10738-031). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, inactive ingredient, dosage & administration, otc - keep out of reach of children, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiseptic
Indications & Usage
Prevents skin infection, removes germs
Warnings
for external use only
Inactive Ingredient
allantoin, aloe barbadensis leaf juice, arginine, caprylyl/capryl glucoside, cetyl hydroxyethylcellulose, citric acid, citrus aurantium dulcis fruit extract, cocamidopropyl betaine, cocamidopropyl hydroxysultaine, decyl glucoside, disodium 2-sulfolaurate, leuconostoc/radish root ferment filtrate, lycium chinensis fruit extract, niacinamide, olea europaea fruit extract, opuntia ficus-indica fruit extract, panthenol, peg-12 dimethicone, potassium sorbate, propanediol, sodium citrate, sodium lauryl sulfocaetate, sodium methyul 2-sulfolaurate, tetrasodium glutamate diacetate, water, zinc pca
Dosage & Administration
spray on affected area, let dry
Otc - 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.
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