NDC 70784-003-01 - Biellee Pollen Whitening Wrinkle Time Repair Serum
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
- 70784-003
- Requested NDC
- 70784-003-01
- Package NDCs from labels
- 70784-003-01, 70784-003-02
- Manufacturer
- NSB CO., LTD.
- Effective date
- 2016-06-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Drug Facts | NSB CO., LTD. | 2016-06-22 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70784-003-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-c4de-f424-e053-dadaa90a57ce | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70784-003-01 | Biellee Pollen Whitening Wrinkle Time Repair Serum | 40 mL in 1 CONTAINER | CREAM | 40 | 1 | |
| 70784-003-02 | Biellee Pollen Whitening Wrinkle Time Repair Serum | 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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| SHINE pH MOISTURE | SODIUM HYALURONATE | CH BIO CO., LTD. | 2f15d0e6-d9e0-3928-e063-6294a90af66f | 2025-02-26 | Warnings | YSE9PPT4TH |
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| SIMETHICONE | SIMETHICONE | NuCare Pharmaceuticals,Inc. | e07f6acc-1b75-d8eb-e053-2a95a90a7d9b | 2025-02-24 | Warnings | 92RU3N3Y1O |
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| SHINE pH ESSENCE | SODIUM HYALURONATE | CH BIO CO., LTD. | 2edc4479-fb5a-d8a9-e063-6394a90a0db3 | 2025-02-23 | Warnings | YSE9PPT4TH |
| Gas relief | SIMETHICONE | Discount Drug Mart, Inc | 2df9117a-97cc-532d-e063-6294a90a1a9c | 2025-02-20 | Warnings | 92RU3N3Y1O |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.