NDC 70519-005-01 - Prestige Caviar Super Aqua Serum
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
- 70519-005
- Requested NDC
- 70519-005-01
- Package NDCs from labels
- 70519-005-01, 70519-005-02
- Manufacturer
- FW1 R&D_Branch | Cosmax, Inc
- Effective date
- 2017-06-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Prestige Caviar Super Aqua Serum - FW1 R&D_Branch | Cosmax, Inc | FW1 R&D_Branch | Cosmax, Inc | 2017-06-27 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70519-005-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-dc25-f424-e053-dadaa90a57ce | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70519-005-01 | Prestige Caviar Super Aqua Serum | 50 mL in 1 CONTAINER | CREAM | 50 | 3 | |
| 70519-005-02 | Prestige Caviar Super Aqua Serum | 1 in 1 PACKAGE | CREAM | 1 | 3 |
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.