warnings
Warnings For external use only: hands Flammable, keep away from fire or flame.
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
- Hand Sanitizer
- Generic name
- ETHYL ALCOHOL
- Manufacturer
- UpLift Brands LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- dd569334-0280-49d6-afcf-0c49ed316cb9
- SPL ID
- 4cc46e58-b3bd-8b30-e063-6294a90a490b
- Version
- 4
- Effective date
- 2026-03-11
- Source export date
- 2026-10-27
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/eeb012fd0992efa4f76b2aef09dd5f84150b96392c46717c44deabcc4e3581c1/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:38:13
| 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 | M505G(a)(3) | openfda.application_number | |
| brand name | Hand Sanitizer | openfda.brand_name | |
| generic name | ETHYL ALCOHOL | openfda.generic_name | |
| manufacturer name | UpLift Brands LLC | openfda.manufacturer_name | |
| ndc | package | 83986-529-50 | openfda.package_ndc |
| ndc | package | 83986-529-32 | openfda.package_ndc |
| ndc | package | 83986-529-16 | openfda.package_ndc |
| ndc | package | 83986-529-34 | openfda.package_ndc |
| ndc | package | 83986-529-86 | openfda.package_ndc |
| ndc | product | 83986-529 | openfda.product_ndc |
| ndc11 | package | 83986052934 | derived:openfda.package_ndc |
| ndc11 | package | 83986052986 | derived:openfda.package_ndc |
| ndc11 | package | 83986052932 | derived:openfda.package_ndc |
| ndc11 | package | 83986052950 | derived:openfda.package_ndc |
| ndc11 | package | 83986052916 | derived:openfda.package_ndc |
| rxcui | 581662 | openfda.rxcui | |
| spl id | 4cc46e58-b3bd-8b30-e063-6294a90a490b | id | |
| spl set id | dd569334-0280-49d6-afcf-0c49ed316cb9 | set_id | |
| unii | 3K9958V90M | 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 www.germx.com Pat. 9,161,982
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.