NDC 55030-003-01 - BlackcurrantEnzymePowder
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
- 55030-003
- Requested NDC
- 55030-003-01
- Package NDCs from labels
- 55030-003-01, 55030-003-02
- Manufacturer
- Shenzhen Aiwei Biological Technology Co., Ltd.
- Effective date
- 2020-06-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| BlackcurrantEnzymePowder - Shenzhen Aiwei Biological Technology Co., Ltd. | Shenzhen Aiwei Biological Technology Co., Ltd. | 2020-06-11 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 55030-003-02 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-5ad1-a426-e053-dadaa90af4c2 | a7cbc688-6b94-f2a8-e053-2995a90aa414 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55030-003-01 | BlackcurrantEnzymePowder | 3 g in 1 PACKAGE | POWDER | 3 | 1 | |
| 55030-003-02 | BlackcurrantEnzymePowder | 15 in 1 PACKAGE, COMBINATION | POWDER | 15 | 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.