Dandruff
- Product NDC
- 59779-836
- 11-digit product format
- 597790836
- Labeler code
- 59779
- Product ID
- 59779-836_01f92a10-4a62-400f-89bc-10edaa9399aa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pyrithione zinc
- Dosage form
- SHAMPOO
- Route
- TOPICAL
- Labeler
- CVS Pharmacy, Inc
- Application
- part358H
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-12-06
- Marketing end
- 0000-00-00
- Substance
- PYRITHIONE ZINC
- Active strength
- 10 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 59779-836 | D | Discontinued by firm | 2026-10-15 | ||
| excluded package | package | 59779-836 | 59779-836-35 | D | Discontinued by firm | 2026-10-15 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded product | product | d630ba8d3edf… | 732f749b63fb… | |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 59779-836-35 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 59779-836-35 | f5e01cc5f278… | a2eaf40c39c3… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 59779-836-35 | 59779083635 | 700 mL in 1 BOTTLE, PLASTIC (59779-836-35) | 700 ml | 2013-12-06 | 0000-00-00 | No | No | Current |