warnings
Warnings For external use only.
BIOPURE 50CT ANTI BACTERIAL HAND WIPES
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
- BIOPURE 50CT ANTI BACTERIAL HAND WIPES
- Generic name
- BENZALKONIUM CHLORIDE
- Manufacturer
- Zhejiang Furuisen Spunlaced Nonwovens Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- ecef31dc-2f36-b578-e053-2995a90a3acd
- SPL ID
- 2d637b1f-5e12-efb1-e063-6394a90af6a8
- Version
- 4
- Effective date
- 2025-02-05
- Source export date
- 2026-10-30
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/e37bebe0ee356110e46fe9b102632217cd5fd64caa93a64cf6ef0d92a0bfdb4c/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:52:52
| 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 | BIOPURE 50CT ANTI BACTERIAL HAND WIPES | openfda.brand_name | |
| generic name | BENZALKONIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Zhejiang Furuisen Spunlaced Nonwovens Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 79794-700-05 | openfda.package_ndc |
| ndc | package | 79794-700-03 | openfda.package_ndc |
| ndc | package | 79794-700-06 | openfda.package_ndc |
| ndc | package | 79794-700-02 | openfda.package_ndc |
| ndc | package | 79794-700-04 | openfda.package_ndc |
| ndc | package | 79794-700-01 | openfda.package_ndc |
| ndc | product | 79794-700 | openfda.product_ndc |
| ndc11 | package | 79794070002 | derived:openfda.package_ndc |
| ndc11 | package | 79794070001 | derived:openfda.package_ndc |
| ndc11 | package | 79794070004 | derived:openfda.package_ndc |
| ndc11 | package | 79794070003 | derived:openfda.package_ndc |
| ndc11 | package | 79794070006 | derived:openfda.package_ndc |
| ndc11 | package | 79794070005 | derived:openfda.package_ndc |
| rxcui | 1038558 | openfda.rxcui | |
| spl id | 2d637b1f-5e12-efb1-e063-6394a90af6a8 | id | |
| spl set id | ecef31dc-2f36-b578-e053-2995a90a3acd | set_id | |
| unii | F5UM2KM3W7 | 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.