Ethyl Alcohol
- Manufacturer
- Chemco Corporation
- Effective date
- 2020-09-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-05-31 23:28:47
Label at a glance#
ProductEthyl Alcohol
Active ingredientALCOHOL
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 49283-700-64 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-7b57-a426-e053-dadaa90af4c2 | 49283-700-64 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49283-700-64 | Ethyl Alcohol | 1892 mL in 1 BOTTLE | GEL | 1892 | 4 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Ethyl Alcohol
- .ALPHA.-HEXYLCINNAMALDEHYDE
- BUTYLPHENYL METHYLPROPIONAL
- ISOMETHYL-.ALPHA.-IONONE
- WATER
- ALCOHOL
- GLYCERIN
- POLYSORBATE 20
- CARBOMER 940
- TROLAMINE
- ISOPROPYL MYRISTATE
- ALPHA-TOCOPHEROL ACETATE
- BENZYL SALICYLATE
- LINALOOL, (+/-)-
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49283-700 | 49283-700-64 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| .ALPHA.-HEXYLCINNAMALDEHYDE | 7X6O37OK2I | IACT |
| BUTYLPHENYL METHYLPROPIONAL | T7540GJV69 | IACT |
| ISOMETHYL-.ALPHA.-IONONE | 9XP4LC555B | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| GLYCERIN | PDC6A3C0OX | IACT |
| POLYSORBATE 20 | 7T1F30V5YH | IACT |
| CARBOMER 940 | 4Q93RCW27E | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| ISOPROPYL MYRISTATE | 0RE8K4LNJS | IACT |
| ALPHA-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| BENZYL SALICYLATE | WAO5MNK9TU | IACT |
| LINALOOL, (+/-)- | D81QY6I88E | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| aed085af-25e5-4ac8-e053-2995a90a0abb | aed085e8-d8aa-671a-e053-2995a90ac9a4 | 2020-09-08 | aed085af-25e5-4ac8-e053-2995a90a0abb aed085e8-d8aa-671a-e053-2995a90ac9a4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
