warnings
Warnings For external use only
Antibacterial
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
- Antibacterial
- Generic name
- BENZALKONIUM CHLORIDE
- Manufacturer
- Sante Manufacturing Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3e64d344-8883-0235-e054-00144ff8d46c
- SPL ID
- 2abd8abc-4e8c-774a-e063-6394a90a23de
- Version
- 5
- Effective date
- 2025-01-02
- Source export date
- 2026-10-27
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/2eee27992d1f29d82f827fd5be42f1314ed39ce4c497af5d81435ac6656a0957/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:22:38
| 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 | Antibacterial | openfda.brand_name | |
| generic name | BENZALKONIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Sante Manufacturing Inc | openfda.manufacturer_name | |
| ndc | package | 71020-004-64 | openfda.package_ndc |
| ndc | product | 71020-004 | openfda.product_ndc |
| ndc11 | package | 71020000464 | derived:openfda.package_ndc |
| rxcui | 1046593 | openfda.rxcui | |
| spl id | 2abd8abc-4e8c-774a-e063-6394a90a23de | id | |
| spl set id | 3e64d344-8883-0235-e054-00144ff8d46c | 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.