Aluroderm Scar
- Product NDC
- 76420-955
- 11-digit product format
- 764200955
- Labeler code
- 76420
- Product ID
- 76420-955_31b18752-52bd-1354-e063-6394a90a31f1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- allantoin
- Dosage form
- PATCH
- Route
- CUTANEOUS
- Labeler
- Asclemed USA, Inc.
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-04-01
- Substance
- ALLANTOIN
- Active strength
- .0075 g/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Aluroderm Scar
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLANTOIN | .0075 g/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 344S277G0Z |
| Rxcui | 2711688 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76420-955-01 | Aluroderm Scar | 1 in 1 BOX | PATCH | 1 | | 1 |
| 76420-955-01 | Aluroderm Scar | 5 in 1 POUCH | PATCH | 5 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76420-955 | ALURODERM SCAR (ALLANTOIN) PATCH [ASCLEMED USA, INC.] | 1 | Current NDC, 2 package rows | 20250403_60656ca1-5218-4595-854e-19f1061def1e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 76420-955-01 | 76420095501 | 1 POUCH in 1 BOX (76420-955-01) / 5 PATCH in 1 POUCH / 8.5 g in 1 PATCH | 1 pouch | 2025-04-01 | No | No | Current |