warnings
Warnings For external use only When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water Stop use and ask a doctor if • irritation or redness develop and condition persists.
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
- Foaming Hand Sanitizer
- Generic name
- HAND SANITIZER
- Manufacturer
- American Chemical Systems II, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3085d595-68b7-4100-81c0-f0699a7609d6
- SPL ID
- dcefd1ab-5791-4e0d-804f-df19590ef8cf
- Version
- 2
- Effective date
- 2025-11-10
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:05:14
| 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 | Foaming Hand Sanitizer | openfda.brand_name | |
| generic name | HAND SANITIZER | openfda.generic_name | |
| manufacturer name | American Chemical Systems II, LLC | openfda.manufacturer_name | |
| ndc | package | 75044-280-16 | openfda.package_ndc |
| ndc | package | 75044-280-31 | openfda.package_ndc |
| ndc | product | 75044-280 | openfda.product_ndc |
| ndc11 | package | 75044028031 | derived:openfda.package_ndc |
| ndc11 | package | 75044028016 | derived:openfda.package_ndc |
| rxcui | 1020365 | openfda.rxcui | |
| spl id | dcefd1ab-5791-4e0d-804f-df19590ef8cf | id | |
| spl set id | 3085d595-68b7-4100-81c0-f0699a7609d6 | 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.