Kleenline Foam Hand Sanitizer
FDA Label NDC 78168-618
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Teh Tung Corporation for the product Kleenline Foam Hand Sanitizer (NDC 78168-618). 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 drug facts, active ingredient, purpose, uses, directions, inactive ingredients, warnings, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzalkonium Chloride 0.13%
Purpose
Antimicrobial
Uses
• Hand sanitizing to help reduce bacteria on the skin
• Recommended for repeated use
Directions
Apply liberally to the hands and gently rub until dry.
Inactive Ingredients
Purified water, D-glucopyranose, Oligomeric, Decyl octyl glycosides, Glycerol, Methylisothiazolinone and Citric acid
Warnings
For external use only.
When using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or redness appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Other Information
Store above 0°C (32°F)
Questions?
Call 1-800-995-4466
Packaging
Image (78168)
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