warnings
Warnings For external use only. When using this product avoid contact with the eyes. In case of eye contact, flush with water. Stop use and ask a doctor if irritation and redness develops.
Dial Complete Antibacterial Bar Spring Water
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
- Dial Complete Antibacterial Bar Spring Water
- Generic name
- BENZALKONIUM CHLORIDE
- Manufacturer
- Henkel Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- bd0db24a-668c-b9d0-e053-2a95a90aafbb
- SPL ID
- 438147b1-c5d8-2bc7-e063-6294a90ad740
- Version
- 10
- Effective date
- 2025-11-13
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:16:46
| 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 | Dial Complete Antibacterial Bar Spring Water | openfda.brand_name | |
| generic name | BENZALKONIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Henkel Corporation | openfda.manufacturer_name | |
| ndc | package | 54340-270-25 | openfda.package_ndc |
| ndc | package | 54340-270-23 | openfda.package_ndc |
| ndc | package | 54340-270-26 | openfda.package_ndc |
| ndc | package | 54340-270-18 | openfda.package_ndc |
| ndc | package | 54340-270-21 | openfda.package_ndc |
| ndc | package | 54340-270-22 | openfda.package_ndc |
| ndc | package | 54340-270-16 | openfda.package_ndc |
| ndc | package | 54340-270-27 | openfda.package_ndc |
| ndc | package | 54340-270-17 | openfda.package_ndc |
| ndc | package | 54340-270-15 | openfda.package_ndc |
| ndc | package | 54340-270-14 | openfda.package_ndc |
| ndc | package | 54340-270-24 | openfda.package_ndc |
| ndc | package | 54340-270-19 | openfda.package_ndc |
| ndc | package | 54340-270-13 | openfda.package_ndc |
| ndc | product | 54340-270 | openfda.product_ndc |
| ndc11 | package | 54340027022 | derived:openfda.package_ndc |
| ndc11 | package | 54340027017 | derived:openfda.package_ndc |
| ndc11 | package | 54340027019 | derived:openfda.package_ndc |
| ndc11 | package | 54340027024 | derived:openfda.package_ndc |
| ndc11 | package | 54340027026 | derived:openfda.package_ndc |
| ndc11 | package | 54340027025 | derived:openfda.package_ndc |
| ndc11 | package | 54340027014 | derived:openfda.package_ndc |
| ndc11 | package | 54340027013 | derived:openfda.package_ndc |
| ndc11 | package | 54340027016 | derived:openfda.package_ndc |
| ndc11 | package | 54340027021 | derived:openfda.package_ndc |
| ndc11 | package | 54340027027 | derived:openfda.package_ndc |
| ndc11 | package | 54340027015 | derived:openfda.package_ndc |
| ndc11 | package | 54340027018 | derived:openfda.package_ndc |
| ndc11 | package | 54340027023 | derived:openfda.package_ndc |
| rxcui | 1926450 | openfda.rxcui | |
| spl id | 438147b1-c5d8-2bc7-e063-6294a90ad740 | id | |
| spl set id | bd0db24a-668c-b9d0-e053-2a95a90aafbb | 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.