warnings
Warnings For external use only. Avoid contact with eyes. If eye contact occurs, flush eyes with water. Stop use if , in rare instances, redness or irritation develops. If condition persists for more than 72 hours, consult a physician.
Foaming Advanced Antibacterial Hand
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
- Foaming Advanced Antibacterial Hand
- Generic name
- BENZALKONIUM CHLORIDE
- Manufacturer
- Kutol Products Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 7abc56b5-4446-4464-9b94-6c55f8bb9b74
- SPL ID
- 298e23fa-a68d-383f-e063-6294a90a2e34
- Version
- 9
- Effective date
- 2024-12-18
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:04:17
| 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 | 505G(a)(3) | openfda.application_number | |
| brand name | Foaming Advanced Antibacterial Hand | openfda.brand_name | |
| generic name | BENZALKONIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Kutol Products Company | openfda.manufacturer_name | |
| ndc | package | 50865-213-52 | openfda.package_ndc |
| ndc | package | 50865-213-13 | openfda.package_ndc |
| ndc | package | 50865-213-41 | openfda.package_ndc |
| ndc | package | 50865-213-50 | openfda.package_ndc |
| ndc | package | 50865-213-24 | openfda.package_ndc |
| ndc | package | 50865-213-17 | openfda.package_ndc |
| ndc | package | 50865-213-78 | openfda.package_ndc |
| ndc | product | 50865-213 | openfda.product_ndc |
| ndc11 | package | 50865021378 | derived:openfda.package_ndc |
| ndc11 | package | 50865021324 | derived:openfda.package_ndc |
| ndc11 | package | 50865021317 | derived:openfda.package_ndc |
| ndc11 | package | 50865021350 | derived:openfda.package_ndc |
| ndc11 | package | 50865021313 | derived:openfda.package_ndc |
| ndc11 | package | 50865021352 | derived:openfda.package_ndc |
| ndc11 | package | 50865021341 | derived:openfda.package_ndc |
| spl id | 298e23fa-a68d-383f-e063-6294a90a2e34 | id | |
| spl set id | 7abc56b5-4446-4464-9b94-6c55f8bb9b74 | 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.