warnings
Warnings
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 |
|---|
| ORAL |
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 | M012 | openfda.application_number | |
| brand name | MUCUS RELIEF | openfda.brand_name | |
| generic name | GUAIFENESIN 400 MG | openfda.generic_name | |
| manufacturer name | Pioneer Life Sciences, LLC | openfda.manufacturer_name | |
| ndc | package | 72090-009-01 | openfda.package_ndc |
| ndc | product | 72090-009 | openfda.product_ndc |
| ndc11 | package | 72090000901 | derived:openfda.package_ndc |
| rxcui | 359601 | openfda.rxcui | |
| spl id | 9f130a45-ac52-42e1-aff0-60eeb6492505 | id | |
| spl set id | 3b7e0ee7-4dda-4bbe-842c-6cbbc208acd5 | set_id | |
| unii | 495W7451VQ | 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.