warnings
Warnings For external use only.
Dial Professional Antibacterial Defense 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 Professional Antibacterial Defense Spring Water
- Generic name
- BENZALKONIUM CHLORIDE
- Manufacturer
- Henkel Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 29644a9d-3954-a6e5-e063-6394a90a82c7
- SPL ID
- 458696c6-881f-d85c-e063-6294a90ac119
- Version
- 2
- Effective date
- 2025-12-09
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:34:40
| 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 Professional Antibacterial Defense Spring Water | openfda.brand_name | |
| brand name | Dial Professional Antibacterial and Sensitive Fragrance Free | openfda.brand_name | |
| brand name | Dial Professional Antibacterial Defense Gold | openfda.brand_name | |
| generic name | BENZALKONIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Henkel Corporation | openfda.manufacturer_name | |
| ndc | package | 54340-121-01 | openfda.package_ndc |
| ndc | package | 54340-302-02 | openfda.package_ndc |
| ndc | package | 54340-309-05 | openfda.package_ndc |
| ndc | package | 54340-302-04 | openfda.package_ndc |
| ndc | package | 54340-309-04 | openfda.package_ndc |
| ndc | package | 54340-302-09 | openfda.package_ndc |
| ndc | package | 54340-302-03 | openfda.package_ndc |
| ndc | package | 54340-302-06 | openfda.package_ndc |
| ndc | package | 54340-302-07 | openfda.package_ndc |
| ndc | package | 54340-309-06 | openfda.package_ndc |
| ndc | package | 54340-302-05 | openfda.package_ndc |
| ndc | package | 54340-309-02 | openfda.package_ndc |
| ndc | package | 54340-121-02 | openfda.package_ndc |
| ndc | package | 54340-302-08 | openfda.package_ndc |
| ndc | package | 54340-309-03 | openfda.package_ndc |
| ndc | package | 54340-309-01 | openfda.package_ndc |
| ndc | package | 54340-302-01 | openfda.package_ndc |
| ndc | product | 54340-309 | openfda.product_ndc |
| ndc | product | 54340-121 | openfda.product_ndc |
| ndc | product | 54340-302 | openfda.product_ndc |
| ndc11 | package | 54340012101 | derived:openfda.package_ndc |
| ndc11 | package | 54340030201 | derived:openfda.package_ndc |
| ndc11 | package | 54340030206 | derived:openfda.package_ndc |
| ndc11 | package | 54340030905 | derived:openfda.package_ndc |
| ndc11 | package | 54340030207 | derived:openfda.package_ndc |
| ndc11 | package | 54340030901 | derived:openfda.package_ndc |
| ndc11 | package | 54340030204 | derived:openfda.package_ndc |
| ndc11 | package | 54340030208 | derived:openfda.package_ndc |
| ndc11 | package | 54340030205 | derived:openfda.package_ndc |
| ndc11 | package | 54340030903 | derived:openfda.package_ndc |
| ndc11 | package | 54340030902 | derived:openfda.package_ndc |
| ndc11 | package | 54340030203 | derived:openfda.package_ndc |
| ndc11 | package | 54340030906 | derived:openfda.package_ndc |
| ndc11 | package | 54340030202 | derived:openfda.package_ndc |
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.