warnings
Warnings For external use only flammable, keep away from fire and flame will produce serious gastric disturbances if taken internally
Isopropyl Rubbing Alcohol 50%
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 50%
- Generic name
- ISOPROPYL ALCOHOL
- Manufacturer
- Home Smart Products
- Product type
- HUMAN OTC DRUG
- SPL set ID
- cfe4fca2-bb20-4ab3-b304-32d9ba0451f6
- SPL ID
- 299e468f-6db8-d58d-e063-6294a90ac6a4
- Version
- 2
- Effective date
- 2024-12-19
- Source export date
- 2026-10-27
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/2c7d3f7bcea1543046130e07dcbaf7eea5fb0ce23f7faa6458d1c6d80c3fa0c3/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:44:17
| 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 50% | openfda.brand_name | |
| generic name | ISOPROPYL ALCOHOL | openfda.generic_name | |
| manufacturer name | Home Smart Products | openfda.manufacturer_name | |
| ndc | package | 52862-022-10 | openfda.package_ndc |
| ndc | package | 52862-022-09 | openfda.package_ndc |
| ndc | package | 52862-022-06 | openfda.package_ndc |
| ndc | package | 52862-022-04 | openfda.package_ndc |
| ndc | package | 52862-022-12 | openfda.package_ndc |
| ndc | package | 52862-022-03 | openfda.package_ndc |
| ndc | package | 52862-022-11 | openfda.package_ndc |
| ndc | product | 52862-022 | openfda.product_ndc |
| ndc11 | package | 52862002209 | derived:openfda.package_ndc |
| ndc11 | package | 52862002203 | derived:openfda.package_ndc |
| ndc11 | package | 52862002210 | derived:openfda.package_ndc |
| ndc11 | package | 52862002211 | derived:openfda.package_ndc |
| ndc11 | package | 52862002206 | derived:openfda.package_ndc |
| ndc11 | package | 52862002204 | derived:openfda.package_ndc |
| ndc11 | package | 52862002212 | derived:openfda.package_ndc |
| rxcui | 616456 | openfda.rxcui | |
| spl id | 299e468f-6db8-d58d-e063-6294a90ac6a4 | id | |
| spl set id | cfe4fca2-bb20-4ab3-b304-32d9ba0451f6 | 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.