warnings
Warnings For external use only Flammable, keep away from fire and flame if taken internally, serious gastric disturbances will result
Isopropyl Rubbing Alcohol 70%
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
- Isopropyl Rubbing Alcohol 70%
- Generic name
- ISOPROPYL ALCOHOL
- Manufacturer
- First Aid Research Corp.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 7d1c0382-31b3-48d0-a514-c5cc45a2299e
- SPL ID
- 298db3fa-b267-ce10-e063-6394a90a6499
- Version
- 2
- Effective date
- 2024-12-18
- 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 06:04:20
| 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 | Isopropyl Rubbing Alcohol 70% | openfda.brand_name | |
| generic name | ISOPROPYL ALCOHOL | openfda.generic_name | |
| manufacturer name | First Aid Research Corp. | openfda.manufacturer_name | |
| ndc | package | 75983-008-01 | openfda.package_ndc |
| ndc | package | 75983-008-07 | openfda.package_ndc |
| ndc | package | 75983-008-02 | openfda.package_ndc |
| ndc | package | 75983-008-06 | openfda.package_ndc |
| ndc | package | 75983-008-04 | openfda.package_ndc |
| ndc | package | 75983-008-05 | openfda.package_ndc |
| ndc | package | 75983-008-03 | openfda.package_ndc |
| ndc | product | 75983-008 | openfda.product_ndc |
| ndc11 | package | 75983000806 | derived:openfda.package_ndc |
| ndc11 | package | 75983000802 | derived:openfda.package_ndc |
| ndc11 | package | 75983000804 | derived:openfda.package_ndc |
| ndc11 | package | 75983000805 | derived:openfda.package_ndc |
| ndc11 | package | 75983000803 | derived:openfda.package_ndc |
| ndc11 | package | 75983000807 | derived:openfda.package_ndc |
| ndc11 | package | 75983000801 | derived:openfda.package_ndc |
| rxcui | 808520 | openfda.rxcui | |
| spl id | 298db3fa-b267-ce10-e063-6394a90a6499 | id | |
| spl set id | 7d1c0382-31b3-48d0-a514-c5cc45a2299e | set_id | |
| unii | ND2M416302 | 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.