warnings
WARNINGS SECTION Caution: Discontinue use and consult a physician if redness or Irritation occurs. When using this product avoid contact with eyes, lips or mucous membranes.
Urevia Plus
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Urevia Plus
- Generic name
- UREA 40%
- Manufacturer
- Blue Heron Pharmaceuticals, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- cfa4a44f-fef8-43be-bd14-7fc765a39ae2
- SPL ID
- ca2df984-73e5-4539-a463-3a1ffc0cafb0
- Version
- 1
- Effective date
- 2026-06-04
- Source export date
- 2026-11-06
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:48:40
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
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 |
|---|---|---|---|
| brand name | Urevia Plus | openfda.brand_name | |
| generic name | UREA 40% | openfda.generic_name | |
| manufacturer name | Blue Heron Pharmaceuticals, LLC | openfda.manufacturer_name | |
| ndc | package | 85622-603-04 | openfda.package_ndc |
| ndc | product | 85622-603 | openfda.product_ndc |
| ndc11 | package | 85622060304 | derived:openfda.package_ndc |
| rxcui | 198342 | openfda.rxcui | |
| spl id | ca2df984-73e5-4539-a463-3a1ffc0cafb0 | id | |
| spl set id | cfa4a44f-fef8-43be-bd14-7fc765a39ae2 | set_id | |
| unii | 8W8T17847W | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.