FluMisch Minoxidil Foam
- Product NDC
- 85212-0001
- 11-digit product format
- 852120001
- Labeler code
- 85212
- Product ID
- 85212-0001_2d34dc32-47d9-590d-e063-6294a90a2f2d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil,Biotin
- Dosage form
- AEROSOL, FOAM
- Route
- EXTRACORPOREAL
- Labeler
- Beijing JUNGE Technology Co., Ltd.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-09-01
- Substance
- BIOTIN; MINOXIDIL
- Active strength
- 5; 5 g/100mL; g/100mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- FluMisch Minoxidil Foam
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BIOTIN | 5 g/100mL |
| MINOXIDIL | 5 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6SO6U10H04, 5965120SH1 |
| Rxcui | 2704021 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85212-0001-1 | FluMisch Minoxidil Foam | 60 mL in 1 BOTTLE, PUMP | AEROSOL, FOAM | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 85212-0001 | FLUMISCH MINOXIDIL FOAM (MINOXIDIL,BIOTIN) AEROSOL, FOAM [BEIJING JUNGE TECHNOLOGY CO., LTD.] | 1 | Current NDC, 1 package rows | 20250206_2d34dc32-47d8-590d-e063-6294a90a2f2d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85212-0001-1 | 85212000101 | 60 mL in 1 BOTTLE, PUMP (85212-0001-1) | 60 ml | 2024-09-01 | No | No | Historical |