NDC 68229-409-01 - Alocane Advanced Scar and Itch
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 68229-409
- Requested NDC
- 68229-409-01
- Package NDCs from labels
- 68229-409-01, 68229-409-02
- Manufacturer
- Quest Products, LLC | Filltech USA, LLC
- Effective date
- 2024-11-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Alocane Advanced Scar and Itch - Quest Products, LLC | Filltech USA, LLC | Quest Products, LLC | Filltech USA, LLC | 2024-11-05 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68229-409-01 | Alocane Advanced Scar and Itch | 20.7 mL in 1 TUBE | GEL | 20.7 | 1 | |
| 68229-409-02 | Alocane Advanced Scar and Itch | 1 in 1 CARTON | GEL | 1 | 1 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.