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Ecolab Inc.
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
- Ecolab Inc.
- Generic name
- BENZALKONIUM CHLORIDE
- Manufacturer
- Ecolab Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 7345c155-b5f2-4d29-b469-1153e103cc89
- SPL ID
- c3563ee3-3a2f-49a3-8fd3-acb3ac951d2c
- Version
- 7
- Effective date
- 2024-07-12
- Source export date
- 2026-10-30
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/3b4c9bc1c064560160661a043b9878894ba805e5e90f4733fb76824b6ba7ac42/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:21:57
| 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 | Ecolab Inc. | openfda.brand_name | |
| generic name | BENZALKONIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Ecolab Inc. | openfda.manufacturer_name | |
| ndc | package | 47593-514-94 | openfda.package_ndc |
| ndc | package | 47593-514-62 | openfda.package_ndc |
| ndc | product | 47593-514 | openfda.product_ndc |
| ndc11 | package | 47593051462 | derived:openfda.package_ndc |
| ndc11 | package | 47593051494 | derived:openfda.package_ndc |
| rxcui | 1603470 | openfda.rxcui | |
| spl id | c3563ee3-3a2f-49a3-8fd3-acb3ac951d2c | id | |
| spl set id | 7345c155-b5f2-4d29-b469-1153e103cc89 | 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.