Kamedis MEN CONTROL Dandruff Free Beard Wash
- Product NDC
- 50718-0037
- 11-digit product format
- 507180037
- Labeler code
- 50718
- Product ID
- 50718-0037_5ca1715c-5297-f56f-e063-6394a90a9b5b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pyrithione Zinc
- Dosage form
- LOTION/SHAMPOO
- Route
- CUTANEOUS
- Labeler
- Kamedis Inc.
- Application
- M032
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-01-12
- Substance
- PYRITHIONE ZINC
- Active strength
- 10 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Kamedis MEN CONTROL Dandruff Free Beard Wash
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| PYRITHIONE ZINC | 10 mg/mL |
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 50718-0037-1 | 50718003701 | 1 BOTTLE in 1 CARTON (50718-0037-1) / 200 mL in 1 BOTTLE | 1 bottle | 2025-01-22 | No | No | Current |