NDC 69978-002-01 - SHINMO SAENGBALEUM TREATMENT
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
- 69978-002
- Requested NDC
- 69978-002-01
- Package NDCs from labels
- 69978-002-01, 69978-002-02
- Manufacturer
- ATEC&CO INC.
- Effective date
- 2015-07-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Drug Facts | ATEC&CO INC. | 2015-07-20 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69978-002-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-f6f7-f424-e053-dadaa90a57ce | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69978-002-01 | SHINMO SAENGBALEUM TREATMENT | 958.50 g in 1 BOTTLE | GEL | 958.50 | 3 | |
| 69978-002-02 | SHINMO SAENGBALEUM TREATMENT | 1 in 1 CARTON | GEL | 1 | 3 |
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.