warnings
Warnings For external use only: hands only
Foaming 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
- Foaming Hand
- Generic name
- BENZALKONIUM CHLORIDE
- Manufacturer
- Nice-Pak Products, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 2002c182-b4a6-4baa-8497-74570713b8bb
- SPL ID
- 4cd559bd-73d9-fdfb-e063-6294a90a0afe
- Version
- 18
- Effective date
- 2026-03-12
- 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 06:17:28
| 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 | Foaming Hand | openfda.brand_name | |
| generic name | BENZALKONIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Nice-Pak Products, LLC | openfda.manufacturer_name | |
| ndc | package | 11344-224-04 | openfda.package_ndc |
| ndc | package | 11344-224-20 | openfda.package_ndc |
| ndc | package | 11344-224-44 | openfda.package_ndc |
| ndc | package | 11344-224-86 | openfda.package_ndc |
| ndc | package | 11344-224-45 | openfda.package_ndc |
| ndc | package | 11344-224-08 | openfda.package_ndc |
| ndc | package | 11344-224-96 | openfda.package_ndc |
| ndc | product | 11344-224 | openfda.product_ndc |
| ndc11 | package | 11344022408 | derived:openfda.package_ndc |
| ndc11 | package | 11344022496 | derived:openfda.package_ndc |
| ndc11 | package | 11344022420 | derived:openfda.package_ndc |
| ndc11 | package | 11344022486 | derived:openfda.package_ndc |
| ndc11 | package | 11344022445 | derived:openfda.package_ndc |
| ndc11 | package | 11344022444 | derived:openfda.package_ndc |
| ndc11 | package | 11344022404 | derived:openfda.package_ndc |
| rxcui | 1020365 | openfda.rxcui | |
| spl id | 4cd559bd-73d9-fdfb-e063-6294a90a0afe | id | |
| spl set id | 2002c182-b4a6-4baa-8497-74570713b8bb | set_id | |
| unii | F5UM2KM3W7 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Adverse event Manufactured By: Vi-Jon, Inc. 8515 Page Ave. St. Louis, Mo 63114 vijonprofessional.com
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.