warnings
For external use only Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Do not use in children less than 2 months of age. Do not use on open wounds.
BIOPURE20CT ANTI BACTERIAL HAND WIPES(2010C)
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
- BIOPURE20CT ANTI BACTERIAL HAND WIPES(2010C)
- Generic name
- ANTIBACTERIAL HAND WIPE
- Manufacturer
- Zhejiang Furuisen Spunlaced Nonwovens Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a9318c76-7c41-1634-e053-2a95a90a6d44
- SPL ID
- edbb4d3a-c368-de6b-e053-2a95a90a81fc
- Version
- 13
- Effective date
- 2026-03-13
- Source export date
- 2026-09-28
- 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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:38:15
| 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 | BIOPURE20CT ANTI BACTERIAL HAND WIPES(807C) | openfda.brand_name | |
| brand name | BIOPURE20CT ANTI BACTERIAL HAND WIPES(2010C) | openfda.brand_name | |
| brand name | BIOPURE20CT ANTI BACTERIAL HAND WIPES(7514C) | openfda.brand_name | |
| generic name | ANTIBACTERIAL HAND WIPE | openfda.generic_name | |
| generic name | HAND WIPES | openfda.generic_name | |
| manufacturer name | Zhejiang Furuisen Spunlaced Nonwovens Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 79794-123-01 | openfda.package_ndc |
| ndc | package | 79794-789-01 | openfda.package_ndc |
| ndc | package | 79794-456-01 | openfda.package_ndc |
| ndc | product | 79794-789 | openfda.product_ndc |
| ndc | product | 79794-456 | openfda.product_ndc |
| ndc | product | 79794-123 | openfda.product_ndc |
| ndc11 | package | 79794078901 | derived:openfda.package_ndc |
| ndc11 | package | 79794012301 | derived:openfda.package_ndc |
| ndc11 | package | 79794045601 | derived:openfda.package_ndc |
| spl id | edbb4d3a-c368-de6b-e053-2a95a90a81fc | id | |
| spl set id | a9318c76-7c41-1634-e053-2a95a90a6d44 | 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.