Active Ingredient - Ethanol
Ethanol
Ethanol
FDA Label NDC 79137-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Golden Leaf Energy for the product Ethanol (NDC 79137-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient - ethanol, warnings, indications & usage, otc - purpose, otc - keep out of reach of children, inactive ingredient, dosage & administration, 96% ethanol - 1000l, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
Drug Facts/Warnings
Indications & Usage
Drug Facts - Indications and usage
Otc - Purpose
Drug Facts - Purpose
Otc - Keep Out Of Reach Of Children
Drug Facts - Keep out of reach of children
Inactive Ingredient
Drug Facts - Inactive Ingredients
Dosage & Administration
Drug Facts - Dosage
96% Ethanol - 1000L
1000 - Ethanol
* Please review the disclaimer below.
