warnings
Drug Facts Box OTC-Warnings Section For external use only
Antiseptic Hand
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
- Antiseptic Hand
- Generic name
- CHLOROXYLENOL
- Manufacturer
- Image Supply, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 7edd2630-bd0b-473f-85ab-34c74e8a3a0f
- SPL ID
- 518c3d6c-f385-3c63-e063-6294a90ab136
- Version
- 4
- Effective date
- 2026-05-11
- Source export date
- 2026-10-12
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:12:13
| 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 | Antiseptic Hand | openfda.brand_name | |
| generic name | CHLOROXYLENOL | openfda.generic_name | |
| manufacturer name | Image Supply, Inc. | openfda.manufacturer_name | |
| ndc | package | 16496-544-14 | openfda.package_ndc |
| ndc | product | 16496-544 | openfda.product_ndc |
| ndc11 | package | 16496054414 | derived:openfda.package_ndc |
| rxcui | 413261 | openfda.rxcui | |
| spl id | 518c3d6c-f385-3c63-e063-6294a90ab136 | id | |
| spl set id | 7edd2630-bd0b-473f-85ab-34c74e8a3a0f | 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.