warnings
Warnings For external use only
Certain Dri Clinical Strength Roll On
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
- Certain Dri Clinical Strength Roll On
- Generic name
- ALUMINUM CHLORIDE
- Manufacturer
- Clarion Brands, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 076320fa-a765-4c78-a1d4-307b30242f9e
- SPL ID
- 46a8b3be-c34a-1c9e-e063-6394a90a2ad7
- Version
- 5
- Effective date
- 2025-12-23
- 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 05:34:42
| 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 | M019 | openfda.application_number | |
| brand name | Certain Dri Clinical Strength Roll On | openfda.brand_name | |
| generic name | ALUMINUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Clarion Brands, LLC | openfda.manufacturer_name | |
| ndc | package | 69693-724-12 | openfda.package_ndc |
| ndc | product | 69693-724 | openfda.product_ndc |
| ndc11 | package | 69693072412 | derived:openfda.package_ndc |
| spl id | 46a8b3be-c34a-1c9e-e063-6394a90a2ad7 | id | |
| spl set id | 076320fa-a765-4c78-a1d4-307b30242f9e | set_id | |
| unii | 3CYT62D3GA | 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.