TriDerma Pressure Sore Relief

Product NDC: 10738-031
11-digit product format: 107380031
Labeler code: 10738
Product ID: 10738-031_49799f70-b826-e9c3-e063-6294a90a3b99
Type: HUMAN OTC DRUG
Nonproprietary name: TriDerma Pressure Sore Relief Wound Cleanser
Dosage form: LIQUID
Route: TOPICAL
Labeler: Genuine Virgin Aloe Corporation
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-01-01
Substance: BENZETHONIUM CHLORIDE
Active strength: .0012 g/g
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: TriDerma Pressure Sore Relief
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZETHONIUM CHLORIDE	.0012 g/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
PH41D05744	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1876355	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
49799f70-b825-e9c3-e063-6294a90a3b99	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10738-031-88	TriDerma Pressure Sore Relief	243 g in 1 BOTTLE, PUMP	LIQUID	243		1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
TriDerma Pressure Sore Relief	TRIDERMA PRESSURE SORE RELIEF WOUND CLEANSER	Genuine Virgin Aloe Corporation	49799f70-b825-e9c3-e063-6294a90a3b99	2026-01-28	Warnings	Exact identifier ndc (product): 10738-031

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
PH41D05744	BENZETHONIUM CHLORIDE	121-54-0	BENZETHONIUM CHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1876355	benzethonium chloride 0.12 % Topical Spray	PSN	49799f70-b825-e9c3-e063-6294a90a3b99	1
1876355	benzethonium chloride 1.2 MG/ML Topical Spray	SCD	49799f70-b825-e9c3-e063-6294a90a3b99	1
1876355	benzethonium chloride 0.12 % Topical Spray	SY	49799f70-b825-e9c3-e063-6294a90a3b99	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
10738-031-88	10738003188	243 g in 1 BOTTLE, PUMP (10738-031-88)	243 g	2025-01-01	No	No	Current