warnings
Warnings For external use only. Keep out of eyes. In case of eye contact immediately flush eyes with water. If irritation persists, get medical attention. If swallowed, contact physician. Flammable, keep away from heat or flames.
Germstar Premium 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
- Germstar Premium Hand Sanitizer
- Generic name
- ETHYL ALCOHOL
- Manufacturer
- Soaptronic LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 489652af-7333-628a-e054-00144ff8d46c
- SPL ID
- 2c7baede-035b-8ba4-e063-6294a90a4a7d
- Version
- 4
- Effective date
- 2025-01-24
- 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 05:20:43
| 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 | Germstar Premium Hand Sanitizer | openfda.brand_name | |
| generic name | ETHYL ALCOHOL | openfda.generic_name | |
| manufacturer name | Soaptronic LLC | openfda.manufacturer_name | |
| ndc | package | 57915-008-03 | openfda.package_ndc |
| ndc | package | 57915-008-01 | openfda.package_ndc |
| ndc | package | 57915-008-04 | openfda.package_ndc |
| ndc | package | 57915-008-05 | openfda.package_ndc |
| ndc | package | 57915-008-02 | openfda.package_ndc |
| ndc | product | 57915-008 | openfda.product_ndc |
| ndc11 | package | 57915000803 | derived:openfda.package_ndc |
| ndc11 | package | 57915000802 | derived:openfda.package_ndc |
| ndc11 | package | 57915000805 | derived:openfda.package_ndc |
| ndc11 | package | 57915000801 | derived:openfda.package_ndc |
| ndc11 | package | 57915000804 | derived:openfda.package_ndc |
| rxcui | 1041807 | openfda.rxcui | |
| spl id | 2c7baede-035b-8ba4-e063-6294a90a4a7d | id | |
| spl set id | 489652af-7333-628a-e054-00144ff8d46c | set_id | |
| unii | 3K9958V90M | 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.