NDC 71702-090-01 - CLEMATIS Morning dew BB 21 Light Beige
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
- 71702-090
- Requested NDC
- 71702-090-01
- Package NDCs from labels
- 71702-090-01, 71702-090-02
- Manufacturer
- Coshub Co., Ltd. | COSON Co., Ltd._Osan Plant
- Effective date
- 2017-09-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Titanium Dioxide - Coshub Co., Ltd. | COSON Co., Ltd._Osan Plant | Coshub Co., Ltd. | COSON Co., Ltd._Osan Plant | 2017-09-05 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71702-090-02 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-3705-a910-e053-dadaa90a0b85 | d4563e37-8cfa-4e77-83da-64118f9912c0 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71702-090-01 | CLEMATIS Morning dew BB 21 Light Beige | 50 mL in 1 TUBE | CREAM | 50 | 1 | |
| 71702-090-02 | CLEMATIS Morning dew BB 21 Light Beige | 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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.