NDC 83767-101-01 - Ruigoo Minoxidil Topical Gel
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
- 83767-101
- Requested NDC
- 83767-101-01
- Package NDCs from labels
- 83767-101-01, 83767-101-02
- Manufacturer
- Guangzhou Ruijiu Electronic Technology Co., Ltd.
- Effective date
- 2024-04-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| RUIGOO MINOXIDIL TOPICAL GEL | Guangzhou Ruijiu Electronic Technology Co., Ltd. | 2024-04-09 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83767-101-01 | Ruigoo Minoxidil Topical Gel | 100 mL in 1 BOTTLE | GEL | 100 | 5 | |
| 83767-101-02 | Ruigoo Minoxidil Topical Gel | 1 in 1 CARTON | GEL | 1 | 5 |
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.