Zinc Pyrithione
- Manufacturer
- CHEMCO CORPORATION
- Effective date
- 2021-04-19
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:39:48
Label at a glance#
ProductZinc Pyrithione
Active ingredientPYRITHIONE ZINC
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 49283-111-10 | 2024-01-30 | C162847 | 48780-1 | 1030e365-12ec-111a-e063-dadaa90a10e2 | 49283-111-10 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49283-111-10 | Zinc Pyrithione | 283 g in 1 BOTTLE | GEL | 283 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Zinc Pyrithione
- SODIUM LAURETH SULFATE
- COCAMIDOPROPYL BETAINE
- COCAMIDOPROPYLAMINE OXIDE
- ALOE VERA LEAF
- PROPYLPARABEN
- METHYLPARABEN
- LINALOOL, (+/-)-
- BUTYLPHENYL METHYLPROPIONAL
- LIMONENE, (+/-)-
- WATER
- PYRITHIONE ZINC
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 900 KD)
- FD&C BLUE NO. 1
- COCAMIDE
- ETHYL ACRYLATE/METHACRYLIC ACID/STEARETH-20 METHACRYLATE COPOLYMER
- DMDM HYDANTOIN
- PHOSPHORIC ACID
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49283-111 | 49283-111-10 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| c053f3a8-4ace-2ead-e053-2995a90a3b7a | bf62ebcb-9b8e-27ec-e053-2995a90a421f | 2021-04-19 | c053f3a8-4ace-2ead-e053-2995a90a3b7a bf62ebcb-9b8e-27ec-e053-2995a90a421f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
