PWMIUHK 5% Minoxidil Topical Solution
- Product NDC
- 84778-081
- 11-digit product format
- 847780081
- Labeler code
- 84778
- Product ID
- 84778-081_3d5b004e-c722-a2fb-e063-6294a90ac39a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- PWMIUHK 5% Minoxidil Topical Solution
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Guangzhou Yixin Cross-border E-commerce Co., Ltd.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-22
- Substance
- MINOXIDIL
- Active strength
- 5 g/100g
- 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
- PWMIUHK 5% Minoxidil Topical Solution
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOXIDIL | 5 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5965120SH1 |
| Rxcui | 311724 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84778-081-01 | PWMIUHK 5% Minoxidil Topical Solution | 60 g in 1 BOTTLE, DROPPER | LIQUID | 60 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84778-081-01 | 84778008101 | 60 g in 1 BOTTLE, DROPPER (84778-081-01) | 60 g | 2025-08-22 | No | No | Historical |