Uses:
To decrease bacteria on the skin.
Benzalkonium Chloride
FDA Label NDC 52305-600
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Freshorize Ltd for the product Benzalkonium Chloride (NDC 52305-600). 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 uses:, warnings, warnings:, directions:, other information:, inactive ingredients:, drug facts, purpose, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
For external use only.
Do not use in eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor is skin irritation develops.
If ingested, get medical help or contact a Poison Control Center immediately.
Warnings:
Keep out of reach of children.
Directions:
Liberally apply product to sin by gently massaging until absorbed.
Supervise children in the use of this product.
Other Information:
Avoid extreme temperatures.
Inactive Ingredients:
Water (Aqua), PEG-40 Hydrogenated Castor Oil, Parfum, Aloe Barbadensis Leaf Extract
Drug Facts
Active Ingredients
Benzalkonium Chloride
Purpose
Antibacterial.
Freshorize Alcohol Free Hand Sanitizer
Requires no water or towels.
Apply small amounts to hands and rub lightly until dry.
www.freshorize.com
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