warnings
Forexternaluse only. Foruse by men only. Extremely Flammable. Avoid fire, flame, or smoking during andimmedlately following application.
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 | 505G(a)(3) | openfda.application_number | |
| brand name | JOHNSON FOAM PRO | openfda.brand_name | |
| generic name | FINASTERIDE FOAM WITH 5% MINOXIDIL | openfda.generic_name | |
| manufacturer name | JOHNSON BIOPHARMACEUTICAL INC. | openfda.manufacturer_name | |
| ndc | package | 84539-002-01 | openfda.package_ndc |
| ndc | product | 84539-002 | openfda.product_ndc |
| ndc11 | package | 84539000201 | derived:openfda.package_ndc |
| spl id | 581d631c-ecc9-940c-e063-6294a90aa0e1 | id | |
| spl set id | 27697b1c-f713-f7e0-e063-6394a90a7514 | set_id | |
| unii | 5965120SH1 | openfda.unii | |
| unii | 57GNO57U7G | 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.