warnings
WARNING KEEP OUT OF REACH OF CHILDREN.
Urea 40%
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
- Urea 40%
- Generic name
- UREA
- Manufacturer
- Patrin Pharma, Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 53ccf801-c1c6-42c8-a511-da33c308076f
- SPL ID
- 2a3a53e2-6a1d-4422-b058-c9799cb3fa79
- Version
- 1
- Effective date
- 2025-08-21
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:46:23
| 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 | Urea 40% | openfda.brand_name | |
| generic name | UREA | openfda.generic_name | |
| manufacturer name | Patrin Pharma, Inc | openfda.manufacturer_name | |
| ndc | package | 39328-019-01 | openfda.package_ndc |
| ndc | package | 39328-019-03 | openfda.package_ndc |
| ndc | package | 39328-019-07 | openfda.package_ndc |
| ndc | product | 39328-019 | openfda.product_ndc |
| ndc11 | package | 39328001901 | derived:openfda.package_ndc |
| ndc11 | package | 39328001903 | derived:openfda.package_ndc |
| ndc11 | package | 39328001907 | derived:openfda.package_ndc |
| rxcui | 198342 | openfda.rxcui | |
| spl id | 2a3a53e2-6a1d-4422-b058-c9799cb3fa79 | id | |
| spl set id | 53ccf801-c1c6-42c8-a511-da33c308076f | set_id | |
| unii | 8W8T17847W | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS Transient stinging, burning, itching or irritation may occur and will normally disappear upon discontinuing the use of this product.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.