warnings
Warnings For external use only: hands only
Hand Wash
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
- Hand Wash
- Generic name
- BENZALKONIUM CHLORIDE
- Manufacturer
- UpLift Brands, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- dd992633-05fd-4544-8abe-e161828a99ad
- SPL ID
- 4cc44476-9723-2d86-e063-6394a90a7905
- Version
- 4
- Effective date
- 2026-03-11
- 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 05:35:41
| 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 | Hand Wash | openfda.brand_name | |
| generic name | BENZALKONIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | UpLift Brands, LLC | openfda.manufacturer_name | |
| ndc | package | 83986-460-96 | openfda.package_ndc |
| ndc | package | 83986-460-08 | openfda.package_ndc |
| ndc | package | 83986-460-04 | openfda.package_ndc |
| ndc | package | 83986-460-45 | openfda.package_ndc |
| ndc | package | 83986-460-44 | openfda.package_ndc |
| ndc | product | 83986-460 | openfda.product_ndc |
| ndc11 | package | 83986046096 | derived:openfda.package_ndc |
| ndc11 | package | 83986046045 | derived:openfda.package_ndc |
| ndc11 | package | 83986046044 | derived:openfda.package_ndc |
| ndc11 | package | 83986046008 | derived:openfda.package_ndc |
| ndc11 | package | 83986046004 | derived:openfda.package_ndc |
| rxcui | 1046593 | openfda.rxcui | |
| spl id | 4cc44476-9723-2d86-e063-6394a90a7905 | id | |
| spl set id | dd992633-05fd-4544-8abe-e161828a99ad | 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 reaction DISTRIBUTED BY: UPLIFT BRANDS, LLC ST. LOUIS, MO 63114 1-866 MY GERMX
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.