warnings
Warnings: For external use only.
Berberex Wound Gel
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
- Berberex Wound Gel
- Generic name
- BENZETHONIUM CHLORIDE, ALLANTOIN
- Manufacturer
- Cosco International, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5dd97e65-bfb3-468e-a2b1-e56d30da99df
- SPL ID
- 67cabb40-44f2-4ad0-ad14-77f4ab2bd1dc
- Version
- 3
- Effective date
- 2025-03-28
- Source export date
- 2026-09-28
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:40:50
| 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 |
|---|---|---|---|
| application number | M003 | openfda.application_number | |
| brand name | Berberex Wound Gel | openfda.brand_name | |
| generic name | BENZETHONIUM CHLORIDE, ALLANTOIN | openfda.generic_name | |
| manufacturer name | Cosco International, Inc. | openfda.manufacturer_name | |
| ndc | package | 52261-0601-1 | openfda.package_ndc |
| ndc | product | 52261-0601 | openfda.product_ndc |
| ndc11 | package | 52261060101 | derived:openfda.package_ndc |
| spl id | 67cabb40-44f2-4ad0-ad14-77f4ab2bd1dc | id | |
| spl set id | 5dd97e65-bfb3-468e-a2b1-e56d30da99df | set_id | |
| unii | PH41D05744 | openfda.unii | |
| unii | 344S277G0Z | 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.