warnings
Warnings Do not use in conjunction Warnings For external use only Do not use in conjunction with products containing acids
finipil Lait 50
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
- finipil Lait 50
- Generic name
- BENZETHONIUM CHLORIDE
- Manufacturer
- Equibal, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- bc630fbc-e428-4d46-8330-fb6f699943fd
- SPL ID
- 461f32f5-973b-7cf2-e063-6294a90a254b
- Version
- 18
- Effective date
- 2025-12-16
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:51
| 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 | finipil Lait 50 | openfda.brand_name | |
| generic name | BENZETHONIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Equibal, Inc. | openfda.manufacturer_name | |
| ndc | package | 53228-050-01 | openfda.package_ndc |
| ndc | product | 53228-050 | openfda.product_ndc |
| ndc11 | package | 53228005001 | derived:openfda.package_ndc |
| spl id | 461f32f5-973b-7cf2-e063-6294a90a254b | id | |
| spl set id | bc630fbc-e428-4d46-8330-fb6f699943fd | set_id | |
| unii | PH41D05744 | 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.