warnings
Warnings : For external use only . Avoid contact with eyes. If contact occurs, rinse Eyes thoroughly with water. If condition worsens or does not improve after regular use of this product as directed, consult a doctor.
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
| Harmonized routes |
|---|
| TOPICAL |
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M032 | openfda.application_number | |
| brand name | MOISTURIZING DANDRUFF 1% Pyrithione Zinc | openfda.brand_name | |
| generic name | PYRITHIONE ZINC | openfda.generic_name | |
| manufacturer name | Bentley Laboratories, LLC | openfda.manufacturer_name | |
| ndc | package | 54111-169-50 | openfda.package_ndc |
| ndc | product | 54111-169 | openfda.product_ndc |
| ndc11 | package | 54111016950 | derived:openfda.package_ndc |
| rxcui | 209884 | openfda.rxcui | |
| spl id | 45ffb481-0a30-b663-e063-6294a90acd45 | id | |
| spl set id | c38b3a45-87f4-4121-8ae6-0a20f7c16c72 | set_id | |
| unii | R953O2RHZ5 | openfda.unii |
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse event summaries are temporarily unavailable. Other product information remains available.