Otc - Active Ingredient
Active Ingredients
Ethyl Alcohol 70% v/v
Saniclean Liquid
FDA Label NDC 63900-150
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Simoniz Saniclean, Llc for the product Saniclean (NDC 63900-150). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antibacterial
Indications & Usage
Uses
To help reduce bacteria on the skin that could cause disease.
Warnings
Warnings
For external use only
FLAMMABLE. Keep Away from heat or flame.
Otc - Do Not Use
Do not use in the eyes or on infants under 6 months of age. If eye contact occurs, flush with water.
Otc - Stop Use
Stop use and ask a doctor if redness and irritation occurs and last for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of the reach of childeren. If swallowed, contact a physician or poison control center.
Dosage & Administration
Directions Apply a small amount to palm. Briskly rub, covering hands with product until dry.
Inactive Ingredient
Inactive ingredients Aloe Barbadensis Leaf Juice, Disodium EDTA, Glycerin, Isopropyl Myristate, PEG-10 Dimethicone, Polyquaternium-11, Tocopheryl Acetate, Water
Other
Simoniz Saniclean, LLC
299 Dividend Road
Rocky Hill, CT 06067
1-800-227-5536
Package Label.Principal Display Panel
Saniclean
Simoniz
Hand Care
Alcohol
Foaming Hand Sanitizer
Manufactured in the U.S.A.
Contents 34 F;. Oz. (1000mL)
* Please review the disclaimer below.
