Active Ingredients
Benzalkonium chloride (0.135%)
Kosette Care Sanitizer
FDA Label NDC 79369-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kosette for the product Kosette Care Sanitizer (NDC 79369-100). 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 ingredients, purpose, keep out of reach of children, uses, warnings, directions, inactive ingredients, kosette care sanitizer spray, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Uses
To decrease bacteria on the skin when soap and water are not available. Recommended for repeated use.
Warnings
For external use only
When using this product avoid contact with eyes. In case of contact with eyes, flush thoroughly with water.
Stop use and ask a doctor if skin irritation or redness develops and lasts.
Keep out of reach of children. If swallowed get medical help or contact a poison control center immediately.
Directions
Spray adequate amount to desired area (clothing or body) at a distance of 6 inches for best result. Avoid spraying onto dark colored clothing.
Inactive Ingredients
Quercus acutissima Sap, Water (Aqua), 1,2-Hexanediol, Propylene Glycol, PEG-60 Hydrogenated Castor Oil, Triethanolamine, Citric Acid, Fragrance (Parfum).
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