warnings
Warnings For external use only; flammable, keep away from fire or flame, heat, spark, electrical
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
- Jell Pharmaceuticals Pvt. Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- cd9884b7-6df3-5ece-e053-2a95a90ab20e
- SPL ID
- 43538073-ad08-2703-e063-6294a90aad13
- Version
- 3
- Effective date
- 2025-11-11
- Source export date
- 2026-11-06
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/f699a9578a0c5d6f5abd59491e85ce3c2c5e4567a51003fee350566c56ba5812/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:32:26
| 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 | Jell Pharmaceuticals Pvt. Ltd. | openfda.manufacturer_name | |
| ndc | package | 30400-504-03 | openfda.package_ndc |
| ndc | package | 30400-504-05 | openfda.package_ndc |
| ndc | package | 30400-504-01 | openfda.package_ndc |
| ndc | package | 30400-504-06 | openfda.package_ndc |
| ndc | package | 30400-504-07 | openfda.package_ndc |
| ndc | package | 30400-504-08 | openfda.package_ndc |
| ndc | package | 30400-504-10 | openfda.package_ndc |
| ndc | package | 30400-504-02 | openfda.package_ndc |
| ndc | package | 30400-504-04 | openfda.package_ndc |
| ndc | product | 30400-504 | openfda.product_ndc |
| ndc11 | package | 30400050406 | derived:openfda.package_ndc |
| ndc11 | package | 30400050404 | derived:openfda.package_ndc |
| ndc11 | package | 30400050405 | derived:openfda.package_ndc |
| ndc11 | package | 30400050401 | derived:openfda.package_ndc |
| ndc11 | package | 30400050407 | derived:openfda.package_ndc |
| ndc11 | package | 30400050410 | derived:openfda.package_ndc |
| ndc11 | package | 30400050408 | derived:openfda.package_ndc |
| ndc11 | package | 30400050403 | derived:openfda.package_ndc |
| ndc11 | package | 30400050402 | derived:openfda.package_ndc |
| rxcui | 808520 | openfda.rxcui | |
| spl id | 43538073-ad08-2703-e063-6294a90aad13 | id | |
| spl set id | cd9884b7-6df3-5ece-e053-2a95a90ab20e | 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.