FDA.reportPublic FDA data

Ethyl Alcohol

Manufacturer
Chemco Corporation
Effective date
2020-07-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:20:20

Label at a glance#

ProductEthyl Alcohol
Active ingredientALCOHOL
Label structure3 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HS ORIGINAL 2OZHS ORIGINAL 2OZMain LabelMain Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ORIGINAL2OZORIGINAL2OZALOE 2OZALOE 2OZ

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HS 18OZHS 18OZ

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN3
581662ethanol 0.7 ML/ML Topical GelSCD3
581662ethanol 70 % Topical GelSY3
581662ethyl alcohol 70 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49283-700-022022-01-28C16284748780-19d75b9d0-b9d7-f424-e053-dadaa90a57ce49283 700-02,08,18 701-02,08,18
49283-700-082022-01-28C16284748780-19d75b9d0-b9d7-f424-e053-dadaa90a57ce49283 700-02,08,18 701-02,08,18
49283-700-182022-01-28C16284748780-19d75b9d0-b9d7-f424-e053-dadaa90a57ce49283 700-02,08,18 701-02,08,18
49283-701-022022-01-28C16284748780-19d75b9d0-b9d7-f424-e053-dadaa90a57ce49283 700-02,08,18 701-02,08,18
49283-701-082022-01-28C16284748780-19d75b9d0-b9d7-f424-e053-dadaa90a57ce49283 700-02,08,18 701-02,08,18
49283-701-182022-01-28C16284748780-19d75b9d0-b9d7-f424-e053-dadaa90a57ce49283 700-02,08,18 701-02,08,18
49283-700-022020-01-31C16284748780-19d75b9d0-b9d7-f424-e053-dadaa90a57ce49283 700-02,08,18 701-02,08,18
49283-700-082020-01-31C16284748780-19d75b9d0-b9d7-f424-e053-dadaa90a57ce49283 700-02,08,18 701-02,08,18
49283-700-182020-01-31C16284748780-19d75b9d0-b9d7-f424-e053-dadaa90a57ce49283 700-02,08,18 701-02,08,18
49283-701-022020-01-31C16284748780-19d75b9d0-b9d7-f424-e053-dadaa90a57ce49283 700-02,08,18 701-02,08,18
49283-701-082020-01-31C16284748780-19d75b9d0-b9d7-f424-e053-dadaa90a57ce49283 700-02,08,18 701-02,08,18
49283-701-182020-01-31C16284748780-19d75b9d0-b9d7-f424-e053-dadaa90a57ce49283 700-02,08,18 701-02,08,18

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49283-700-02Ethyl Alcohol59 mL in 1 BOTTLE, PUMPGEL593
49283-700-08Ethyl Alcohol236 mL in 1 BOTTLE, PUMPGEL2363
49283-700-18Ethyl Alcohol532 mL in 1 BOTTLE, PUMPGEL5323
49283-701-02Ethyl Alcohol59 mL in 1 BOTTLE, PUMPGEL593
49283-701-08Ethyl Alcohol236 mL in 1 BOTTLE, PUMPGEL2363
49283-701-18Ethyl Alcohol532 mL in 1 BOTTLE, PUMPGEL5323

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49283-700ETHYL ALCOHOL GEL [CHEMCO CORPORATION]3Legacy NDC, 3 package rows20200708_3d2fd563-2aa0-4fea-e054-00144ff88e88.zip
49283-701ETHYL ALCOHOL GEL [CHEMCO CORPORATION]3Legacy NDC, 3 package rows20200708_3d2fd563-2aa0-4fea-e054-00144ff88e88.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49283-70149283-701-02, 49283-701-08, 49283-701-18
49283-70049283-700-02, 49283-700-08, 49283-700-18

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
POLYSORBATE 207T1F30V5YHIACT
CARBOMER 9404Q93RCW27EIACT
TROLAMINE9O3K93S3TKIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
BENZYL SALICYLATEWAO5MNK9TUIACT
LINALOOL, (+/-)-D81QY6I88EIACT
GLYCERINPDC6A3C0OXIACT
POLYSORBATE 207T1F30V5YHIACT
CARBOMER 9404Q93RCW27EIACT
TROLAMINE9O3K93S3TKIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
LINALOOL, (+/-)-D81QY6I88EIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a9dc9c78-3f20-e007-e053-2995a90afe673d2fd563-2aa0-4fea-e054-00144ff88e882020-07-07Exact identifier
spl id: a9dc9c78-3f20-e007-e053-2995a90afe67
spl set id: 3d2fd563-2aa0-4fea-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.