warnings
Warnings For external use only: hands Flammable, keep away from fire or flame.
Advanced 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
- Advanced Hand Sanitizer
- Generic name
- ETHYL ALCOHOL
- Manufacturer
- Meijer, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a56b4a66-3923-4e40-a461-1d97043fb89a
- SPL ID
- 4b33a939-c22a-ff10-e063-6294a90adca5
- Version
- 20
- Effective date
- 2026-02-19
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:55:14
| 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 | 505G(a)(3) | openfda.application_number | |
| brand name | Advanced Hand Sanitizer | openfda.brand_name | |
| generic name | ETHYL ALCOHOL | openfda.generic_name | |
| manufacturer name | Meijer, Inc. | openfda.manufacturer_name | |
| ndc | package | 41250-370-45 | openfda.package_ndc |
| ndc | package | 41250-370-16 | openfda.package_ndc |
| ndc | package | 41250-370-34 | openfda.package_ndc |
| ndc | package | 41250-370-06 | openfda.package_ndc |
| ndc | product | 41250-370 | openfda.product_ndc |
| ndc11 | package | 41250037045 | derived:openfda.package_ndc |
| ndc11 | package | 41250037016 | derived:openfda.package_ndc |
| ndc11 | package | 41250037006 | derived:openfda.package_ndc |
| ndc11 | package | 41250037034 | derived:openfda.package_ndc |
| rxcui | 581662 | openfda.rxcui | |
| spl id | 4b33a939-c22a-ff10-e063-6294a90adca5 | id | |
| spl set id | a56b4a66-3923-4e40-a461-1d97043fb89a | 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 Pat. 9, 161, 982 Questions 1-888-593-0593 DIST. BY MEIJER DISTRIBUTION, INC. GRAND RAPIDS, MI 49544 www.meijer.com
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.