Medicasp Anti-Dandruff
- Product NDC
- 50066-040
- 11-digit product format
- 500660040
- Labeler code
- 50066
- Product ID
- 50066-040_f59c3b9a-dfb4-4621-8874-70c591ce61ee
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- COAL TAR
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Genomma Lab USA
- Application
- M032
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-11-25
- Substance
- COAL TAR
- Active strength
- 5 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Medicasp Anti-Dandruff
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| COAL TAR | 5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | R533ESO2EC |
| Rxcui | 309381, 2610995 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50066-040-06 | Medicasp Anti-Dandruff | 1 in 1 CARTON | LIQUID | 1 | | 1 |
| 50066-040-06 | Medicasp Anti-Dandruff | 177 mL in 1 BOTTLE, PLASTIC | LIQUID | 177 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50066-040-06 | 50066004006 | 1 BOTTLE, PLASTIC in 1 CARTON (50066-040-06) / 177 mL in 1 BOTTLE, PLASTIC | 2025-11-25 | No | No | Current |