URBAN WASH DANDRUFF
- Product NDC
- 80801-101
- 11-digit product format
- 808010101
- Labeler code
- 80801
- Product ID
- 80801-101_5b2e709c-6c73-3bb9-e063-6394a90a407e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- pyrithione zinc
- Dosage form
- SHAMPOO
- Route
- TOPICAL
- Labeler
- Primal Elements
- Application
- M032
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-05-01
- Substance
- PYRITHIONE ZINC
- Active strength
- .3 g/100mL
- 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
- URBAN WASH DANDRUFF
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| PYRITHIONE ZINC | .3 g/100mL |
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 |
|---|---|---|---|---|---|---|---|
| 80801-101-01 | 80801010101 | 355 mL in 1 BOTTLE, PLASTIC (80801-101-01) | 355 ml | 2023-05-01 | No | No | Current |