Active Ingredient(S)
Benzalkonium Chloride 0.12%
Antibacterial Hand Wipes
FDA Label NDC 79866-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Osike Cosmetics Co., Ltd. for the product Antibacterial Hand Wipes (NDC 79866-005). 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(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, 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
Purpose
Antimicroblal
Use
●Hand sanitizer to help reduce bacteria
●For use when soap and water are not available.
Warnings
For external use only.
Do Not Use
●on children less than 2 months old.
●on open skin wounds
Otc - When Using
When using this product do not get in eyes. If
contact is made rinse thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash 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 right away.
Directions
●Apply to hands, allow to air dry without wiping.
●Children under 6 years of age should be supervised when using this product
Other Information
●Store in a cool,dry place.
●Avoid freezing and excessive heat.
Inactive Ingredients
Glycerin, Phenoxyethanol, Propylene Glycol, Purified Water
* Please review the disclaimer below.
