warnings
Warnings For external use only. Flammable. Keep away from heat or flame
Instant Hand Sanitizeing Wipe
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
- Instant Hand Sanitizeing Wipe
- Generic name
- ISOPROPANOL AND COMPOUND DOUBLE-STRANDED QUATERNARY AMMONIUM SALTS
- Manufacturer
- Shandong Yayun Sanitary Products Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- aa0dc01a-2c6b-7402-e053-2a95a90af6a2
- SPL ID
- 2778cad1-2929-fab8-e063-6294a90a2fc7
- Version
- 6
- Effective date
- 2024-11-21
- Source export date
- 2026-10-30
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:26:47
| 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 | Instant Hand Sanitizeing Wipe | openfda.brand_name | |
| generic name | ISOPROPANOL AND COMPOUND DOUBLE-STRANDED QUATERNARY AMMONIUM SALTS | openfda.generic_name | |
| manufacturer name | Shandong Yayun Sanitary Products Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 79539-002-17 | openfda.package_ndc |
| ndc | package | 79539-002-08 | openfda.package_ndc |
| ndc | package | 79539-002-22 | openfda.package_ndc |
| ndc | package | 79539-002-16 | openfda.package_ndc |
| ndc | package | 79539-002-19 | openfda.package_ndc |
| ndc | package | 79539-002-06 | openfda.package_ndc |
| ndc | package | 79539-002-20 | openfda.package_ndc |
| ndc | package | 79539-002-05 | openfda.package_ndc |
| ndc | package | 79539-002-03 | openfda.package_ndc |
| ndc | package | 79539-002-12 | openfda.package_ndc |
| ndc | package | 79539-002-23 | openfda.package_ndc |
| ndc | package | 79539-002-18 | openfda.package_ndc |
| ndc | package | 79539-002-09 | openfda.package_ndc |
| ndc | package | 79539-002-15 | openfda.package_ndc |
| ndc | package | 79539-002-24 | openfda.package_ndc |
| ndc | package | 79539-002-07 | openfda.package_ndc |
| ndc | package | 79539-002-13 | openfda.package_ndc |
| ndc | package | 79539-002-21 | openfda.package_ndc |
| ndc | package | 79539-002-02 | openfda.package_ndc |
| ndc | package | 79539-002-10 | openfda.package_ndc |
| ndc | package | 79539-002-04 | openfda.package_ndc |
| ndc | package | 79539-002-11 | openfda.package_ndc |
| ndc | package | 79539-002-14 | openfda.package_ndc |
| ndc | package | 79539-002-01 | openfda.package_ndc |
| ndc | product | 79539-002 | openfda.product_ndc |
| ndc11 | package | 79539000224 | derived:openfda.package_ndc |
| ndc11 | package | 79539000221 | derived:openfda.package_ndc |
| ndc11 | package | 79539000212 | derived:openfda.package_ndc |
| ndc11 | package | 79539000201 | derived:openfda.package_ndc |
| ndc11 | package | 79539000205 | derived:openfda.package_ndc |
| ndc11 | package | 79539000208 | derived:openfda.package_ndc |
| ndc11 | package | 79539000219 | derived:openfda.package_ndc |
| ndc11 | package | 79539000209 | derived:openfda.package_ndc |
| ndc11 | package | 79539000218 | derived:openfda.package_ndc |
| ndc11 | package | 79539000223 | derived:openfda.package_ndc |
| ndc11 | package | 79539000216 | derived:openfda.package_ndc |
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.