TriDerma Foot Defense
- Product NDC
- 10738-064
- 11-digit product format
- 107380064
- Labeler code
- 10738
- Product ID
- 10738-064_49784015-9dd8-090d-e063-6294a90a88e4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TriDerma Foot Defense Cream
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Genuine Virgin Aloe Corporation
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-05-31
- Substance
- ALLANTOIN
- Active strength
- 15 mg/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 Foot Defense
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLANTOIN | 15 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 344S277G0Z |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10738-064-40 | TriDerma Foot Defense | 1 in 1 CARTON | CREAM | 1 | | 1 |
| 10738-064-45 | TriDerma Foot Defense | 119 g in 1 TUBE | CREAM | 119 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 10738-064-40 | 10738006440 | 1 TUBE in 1 CARTON (10738-064-40) / 119 g in 1 TUBE (10738-064-45) | 1 tube | 2025-05-31 | No | No | Historical |
| 10738-064-45 | 10738006445 | 119 g in 1 TUBE | 119 g | | | | Historical |