NDC 51523-112-01 - FACE IT Radiance Two Way Cake NB21
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
- 51523-112
- Requested NDC
- 51523-112-01
- Package NDCs from labels
- 51523-112-01, 51523-112-02
- Manufacturer
- THEFACESHOP CO., LTD
- Effective date
- 2011-09-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| FACE IT Radiance Two Way Cake NB21 - THEFACESHOP CO., LTD | THEFACESHOP CO., LTD | 2011-09-01 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 51523-112-02 | 2019-10-29 | C162847 | 48780-1 | 960f7f55-da2a-8e05-e053-dbdaa90a074a | FACE IT Radiance Two Way Cake NB21 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51523-112-01 | FACE IT Radiance Two Way Cake NB21 | 11 g in 1 CONTAINER | POWDER | 11 | 1 | |
| 51523-112-02 | FACE IT Radiance Two Way Cake NB21 | 1 in 1 BOX | POWDER | 1 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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.