NDC 82038-005-01 - Protectif Deep Tint
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
- 82038-005
- Requested NDC
- 82038-005-01
- Package NDCs from labels
- 82038-005-01, 82038-005-02, 82038-005-03, 82038-005-04
- Manufacturer
- Derma Research Group Inc.
- Effective date
- 2024-05-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Drug Facts | Derma Research Group Inc. | 2024-05-30 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82038-005-01 | Protectif Deep Tint | 100 g in 1 BOTTLE, PUMP | CREAM | 100 | 1 | |
| 82038-005-02 | Protectif Deep Tint | 1 in 1 CARTON | CREAM | 1 | 1 | |
| 82038-005-03 | Protectif Deep Tint | 30 g in 1 BOTTLE, PUMP | CREAM | 30 | 1 | |
| 82038-005-04 | Protectif Deep Tint | 1 in 1 CARTON | CREAM | 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.