NDC 70949-100-01 - Bellido Hydro Secret Ampoule
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
- 70949-100
- Requested NDC
- 70949-100-01
- Package NDCs from labels
- 70949-100-01, 70949-100-02
- Manufacturer
- C MAX Korea Co., Ltd
- Effective date
- 2016-09-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Bellido Hydro Secret Ampoule - C MAX Korea Co., Ltd | C MAX Korea Co., Ltd | 2016-09-12 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70949-100-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-2005-f424-e053-dadaa90a57ce | Bellido Hydro Secret Ampoule |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70949-100-01 | Bellido Hydro Secret Ampoule | 50 mL in 1 AMPULE | LIQUID | 50 | 3 | |
| 70949-100-02 | Bellido Hydro Secret Ampoule | 1 in 1 PACKAGE | LIQUID | 1 | 3 |
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.