Active Ingredient
Active Ingredient
Ethyl Alcohol 70%
Advanced Alcohol Gel Sanitizer Gel
FDA Label NDC 65601-801
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Betco Corporation, Ltd for the product Advanced Alcohol Gel Sanitizer (NDC 65601-801). 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, uses, purpose, warnings, directions, inactive ingredients, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
Uses
• Hand sanitizer to reduce microorganisms on the skin.
• Use this product when soap and water are not available.
Purpose
Purpose
Antiseptic
Warnings
Warnings
• For external use only.
• Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
• FLAMMABLE. This product contains ethyl alcohol. Keep away from
sources of ignition.
• Discontinue use if irritation or redness develops.
• If irritation persists for more than 72 hours, consult a physician.
• KEEP OUT OF REACH OF CHILDREN.
• If swallowed, get medical help or contact a Poison Control Center right away.
KEEP OUT OF REACH OF CHILDREN.
Directions
Directions
• Read the entire label before using this product.
• Place enough product on your palm to thoroughly cover your hands.
• Rub hands together briskly until dry.
Inactive Ingredients
Inactive Ingredients
Water, PEG/PPG-8/3 Laurate, Gycerin, Carbomer, Tetrahydroxypropylethylendiamine, Fragrance.
Principal Display Panel
Advancedalcoholgelsanitizer (Advancedalcoholgelsanitizer)
* Please review the disclaimer below.
