warnings
Drug Facts Box OTC-Warnings Section For external use only
QS Plus Plus Instant Hand Sanitizer
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
- QS Plus Plus Instant Hand Sanitizer
- Generic name
- BENZEALKONIUM CHLORIDE
- Manufacturer
- ABC Compounding Co., Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 343f9139-47bc-44b0-9da1-d9d6f6334bc7
- SPL ID
- 47b98679-150e-8b97-e063-6394a90a82e6
- Version
- 8
- Effective date
- 2026-01-06
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:18:56
| 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 | M004 | openfda.application_number | |
| brand name | QS Plus Plus Instant Hand Sanitizer | openfda.brand_name | |
| generic name | BENZEALKONIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | ABC Compounding Co., Inc. | openfda.manufacturer_name | |
| ndc | package | 62257-457-12 | openfda.package_ndc |
| ndc | package | 62257-457-24 | openfda.package_ndc |
| ndc | package | 62257-457-55 | openfda.package_ndc |
| ndc | package | 62257-457-10 | openfda.package_ndc |
| ndc | package | 62257-457-18 | openfda.package_ndc |
| ndc | package | 62257-457-19 | openfda.package_ndc |
| ndc | package | 62257-457-14 | openfda.package_ndc |
| ndc | package | 62257-457-17 | openfda.package_ndc |
| ndc | package | 62257-457-15 | openfda.package_ndc |
| ndc | package | 62257-457-16 | openfda.package_ndc |
| ndc | product | 62257-457 | openfda.product_ndc |
| ndc11 | package | 62257045714 | derived:openfda.package_ndc |
| ndc11 | package | 62257045717 | derived:openfda.package_ndc |
| ndc11 | package | 62257045712 | derived:openfda.package_ndc |
| ndc11 | package | 62257045710 | derived:openfda.package_ndc |
| ndc11 | package | 62257045719 | derived:openfda.package_ndc |
| ndc11 | package | 62257045755 | derived:openfda.package_ndc |
| ndc11 | package | 62257045718 | derived:openfda.package_ndc |
| ndc11 | package | 62257045724 | derived:openfda.package_ndc |
| ndc11 | package | 62257045715 | derived:openfda.package_ndc |
| ndc11 | package | 62257045716 | derived:openfda.package_ndc |
| rxcui | 1049254 | openfda.rxcui | |
| spl id | 47b98679-150e-8b97-e063-6394a90a82e6 | id | |
| spl set id | 343f9139-47bc-44b0-9da1-d9d6f6334bc7 | set_id | |
| unii | F5UM2KM3W7 | 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.