Antiseptic Foaming 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
- Antiseptic Foaming Hand Sanitizer
- Generic name
- BENZALKONIUM CHLORIDE
- Manufacturer
- Target Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 93d6e4df-9428-4557-b251-c7aa9bda3412
- SPL ID
- 4b1f871e-4c37-6d61-e063-6294a90ae28e
- Version
- 4
- Effective date
- 2026-02-18
- Source export date
- 2026-10-12
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:57:51
| 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 | Antiseptic Foaming Hand Sanitizer | openfda.brand_name | |
| generic name | BENZALKONIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Target Corporation | openfda.manufacturer_name | |
| ndc | package | 82442-812-20 | openfda.package_ndc |
| ndc | product | 82442-812 | openfda.product_ndc |
| ndc11 | package | 82442081220 | derived:openfda.package_ndc |
| rxcui | 1020365 | openfda.rxcui | |
| spl id | 4b1f871e-4c37-6d61-e063-6294a90ae28e | id | |
| spl set id | 93d6e4df-9428-4557-b251-c7aa9bda3412 | set_id | |
| unii | F5UM2KM3W7 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings For external use only – hands only
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Adverse Reaction Dist. by Target Corporation Minneapolis, MN 55403 Made in U.S.A. with U.S. and foreign components. TM & ©2024 Target Brands, Inc. Guest Services 1-800-910-6874
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.