NDC 71702-110-01 - CLEMATIS Morning Dew CC
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
- 71702-110
- Requested NDC
- 71702-110-01
- Package NDCs from labels
- 71702-110-01, 71702-110-02
- 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 |
|---|---|---|---|
| CLEMATIS Morning Dew CC - 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 |
|---|---|---|---|---|---|
| 71702-110-02 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-2cac-a910-e053-dadaa90a0b85 | 655d52ed-976c-4f22-94c4-667a188012b2 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71702-110-01 | CLEMATIS Morning Dew CC | 50 mL in 1 TUBE | CREAM | 50 | 1 | |
| 71702-110-02 | CLEMATIS Morning Dew CC | 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.