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 Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | PH41D05744 |
| Rxcui | 1876355 |
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 |
DailyMed RxNorm Mappings#
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 | Historical |