Aluroderm Scar
- Product NDC
- 84991-0316
- 11-digit product format
- 849910316
- Labeler code
- 84991
- Product ID
- 84991-0316_2d94d970-563c-466c-e063-6294a90a93db
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- allantoin
- Dosage form
- PATCH
- Route
- CUTANEOUS
- Labeler
- Olakino Therapeutics LLC
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-12-24
- Substance
- ALLANTOIN
- Active strength
- .0075 g/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 344S277G0Z | ALLANTOIN | 97-59-6 | ALLANTOIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84991-0316-1 | 84991031601 | 1 POUCH in 1 BOX (84991-0316-1) / 5 PATCH in 1 POUCH / 8.5 g in 1 PATCH | 1 pouch | 2024-12-24 | No | No | Historical |
| 84991-0316-5 | 84991031605 | 5 PATCH in 1 POUCH (84991-0316-5) / 8.5 g in 1 PATCH | 5 patch | 2024-12-24 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Aluroderm Scar Patch | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2025-04-01 | HUMAN OTC DRUG LABEL | 1 |
| Aluroderm Scar Patch | Olakino Therapeutics LLC | 2025-02-07 | HUMAN OTC DRUG LABEL | 2 |