Active Ingredient
Ethyl Alcohol 70% V/V
Ethanol Soap
FDA Label NDC 53125-803
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Superior Chemical Co Dba Northwoods for the product Ethanol (NDC 53125-803). 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, warning statement, purpose, when using directions, inactive ingredients, keep out of reach of children wording, directions for usage and dosage, indications and usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warning Statement
Fore external use only. FLAMMABLE. This product contains ethyl alcohol. Keep away from heat or flame
Purpose
Antiseptic
When Using Directions
when using this product avoid contact with eyes. if contact occurs, rinsth thoroughly wiht water.
Stop use and ask a doctor if irriataion or rash occurs
Inactive Ingredients
Aloe Barbadensis Leaf Juide, D&C Green #5, Fragrance, PER-10 Acrylate/perfluorohexylethly Acrylate copolymer, Perfluoroheexylethyl alcohol, propylene glycol, water
Keep Out Of Reach Of Children Wording
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions For Usage And Dosage
Read entire label before using this product
Place enough product on your palm to thoroughly cover your hands. Rub hands together briskly until dry
Indications And Usage
Hand sanitizer to reduce microorganisms on the skin.
Use this product when soap and water are not available
* Please review the disclaimer below.
