TRIDERMA PRESSURE SORE RELIEF- triderma pressure sore relief wound cleanser liquid

TriDerma Pressure Sore Relief by

Drug Labeling and Warnings

TriDerma Pressure Sore Relief by is a Otc medication manufactured, distributed, or labeled by Genuine Virgin Aloe Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzethonium Chloride 0.12%

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

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TRIDERMA PRESSURE SORE RELIEF 
triderma pressure sore relief wound cleanser liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10738-031
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.0012 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10738-031-88	243 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/01/2025

Labeler - Genuine Virgin Aloe Corporation (961374147)

Establishment
Name	Address	ID/FEI	Business Operations
Genuine Virgin Aloe Corporation		961374147	manufacture(10738-031)