Pureskin Bed and Pressure Sore
- Product NDC
- 87217-001
- 11-digit product format
- 872170001
- Labeler code
- 87217
- Product ID
- 87217-001_461a1c95-6565-9dd8-e063-6294a90a83e7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allantoin
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- BENLONG HALL LLC
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-16
- Substance
- ALLANTOIN
- Active strength
- .6 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pureskin Bed and Pressure Sore
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLANTOIN | .6 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 344S277G0Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87217-001-01 | Pureskin Bed and Pressure Sore | 141 g in 1 JAR | CREAM | 141 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87217-001-01 | 87217000101 | 141 g in 1 JAR (87217-001-01) | 141 g | 2025-12-16 | No | No | Historical |