Active Ingredient
Benzalkonium Chloride 0.13%
Eenk Sanitizer Wipes
FDA Label NDC 81635-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cleaniz Group Llc for the product Eenk Sanitizer Wipes (NDC 81635-001). 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, purpose, use, warnings, otc - stop use, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
■ To decrease bacteria on the skin that could cause disease
Warnings
For external use only
Do not use
In children less than two monthsof age.
On open skin wounds
When using this product, keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Open package, pull wipe. Close package to retain moisture. Wet hands thoroughly with product. Allow to dry without rinsing
Supervise children under six years of age when using this product to avoid swallowing
Other Information
Keep container tightly closed in a dry, cool, and well ventilated place.
Recommended storage temperature: 32F to 104F (0C to 40C)
Inactive Ingredients
Alow Barbadensis leaf jiuce, Phenoxyethanol, Polysorbate 20, Propylene glycol, Tocopheryl Acetate, Water
Package Label.Principal Display Panel
Image Description (Img 6034)
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