Dandruff
- Product NDC
- 70000-0775
- 11-digit product format
- 700000775
- Labeler code
- 70000
- Product ID
- 70000-0775_5c152fef-2185-5b50-e063-6294a90af8db
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pyrithione Zinc
- Dosage form
- LOTION/SHAMPOO
- Route
- TOPICAL
- Labeler
- CARDINAL HEALTH 110, LLC. DBA LEADER
- Application
- M032
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-10
- 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
- Dandruff
- 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 |
|---|---|---|---|---|---|---|---|
| 70000-0775-1 | 70000077501 | 369 mL in 1 BOTTLE, PLASTIC (70000-0775-1) | 369 ml | 2026-09-10 | No | No | Current |