warnings
Warnings For external use only. When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Discontinue use if irritation occurs.
Mckesson Hand Cleanse and Soothe with Aloe
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
- Mckesson Hand Cleanse and Soothe with Aloe
- Generic name
- CHLOROXYLENOL
- Manufacturer
- Mckesson Medical-Surgical Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 075cd889-948a-49dd-8927-e22f7a5bff99
- SPL ID
- 2424a55c-bc9e-7509-e063-6394a90a5552
- Version
- 8
- Effective date
- 2024-10-10
- Source export date
- 2026-11-06
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/f699a9578a0c5d6f5abd59491e85ce3c2c5e4567a51003fee350566c56ba5812/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:30:35
| 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 | Mckesson Hand Cleanse and Soothe with Aloe | openfda.brand_name | |
| generic name | CHLOROXYLENOL | openfda.generic_name | |
| manufacturer name | Mckesson Medical-Surgical Inc. | openfda.manufacturer_name | |
| ndc | package | 68599-5204-2 | openfda.package_ndc |
| ndc | package | 68599-5204-1 | openfda.package_ndc |
| ndc | package | 68599-5204-4 | openfda.package_ndc |
| ndc | package | 68599-5204-5 | openfda.package_ndc |
| ndc | package | 68599-5204-3 | openfda.package_ndc |
| ndc | product | 68599-5204 | openfda.product_ndc |
| ndc11 | package | 68599520405 | derived:openfda.package_ndc |
| ndc11 | package | 68599520404 | derived:openfda.package_ndc |
| ndc11 | package | 68599520402 | derived:openfda.package_ndc |
| ndc11 | package | 68599520401 | derived:openfda.package_ndc |
| ndc11 | package | 68599520403 | derived:openfda.package_ndc |
| spl id | 2424a55c-bc9e-7509-e063-6394a90a5552 | id | |
| spl set id | 075cd889-948a-49dd-8927-e22f7a5bff99 | set_id | |
| unii | 0F32U78V2Q | 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.