NDC 87507-002-01 - MENOKIN 30 SECONDS GLOW AND CLEAR Gel SUNSCREEN BRIGHT
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
- 87507-002
- Requested NDC
- 87507-002-01
- Package NDCs from labels
- 87507-002-01, 87507-002-02
- Manufacturer
- Forest Avenue Co., Ltd. | Cit Co., Ltd.
- Effective date
- 2026-04-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| 87507-002_MENOKIN 30 SECONDS GLOW AND CLEAR GEL SUNSCREEN BRIGHT | Forest Avenue Co., Ltd. | Cit Co., Ltd. | 2026-04-01 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 87507-002-01 | MENOKIN 30 SECONDS GLOW AND CLEAR Gel SUNSCREEN BRIGHT | 50 mL in 1 TUBE | CREAM | 50 | 1 | |
| 87507-002-02 | MENOKIN 30 SECONDS GLOW AND CLEAR Gel SUNSCREEN BRIGHT | 1 in 1 CARTON | CREAM | 1 | 1 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.