United States · FDA National Drug Code directory
DANDRX ANTI-DANDRUFF
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 85521-002_399fb50f-3b1f-3777-e063-6294a90a60ef
- Product NDC
- 85521-002
- Form
- SHAMPOO
- Composition / generic term
- Zinc Pyrithione
- Labeler
- dandRX LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20250730
- Source listing expiry
- 20261231
Source-listed ingredients
- PYRITHIONE ZINC — 2 g/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 237 mL in 1 BOTTLE (85521-002-08) · 85521-002-08
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →