Active Ingredient
Active ingredient. Ethyl Alcohol 70% v/v
Sangel
FDA Label NDC 80314-0002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Acabados Gomaplus S.a. De C.v. for the product Sangel (NDC 80314-0002). 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, purpose, indications and usage, dosage and administration, warnings and precautions, warnings, keep out of reach of children, stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Purpose Antmicrobial
Indications And Usage
Use[s]
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Dosage And Administration
Directions
Place enough product on hands to cover all surfaces. Rub hands together until dry.
Warnings And Precautions
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Children under 6 years of age should be supervised when using.
Warnings
Warnings
For external use only. Flammable. Keep away from heat or flame
Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get
Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Inactive Ingredients
Inactive ingredients Water, Glycerin, Carbomer, Triethanolamine
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