Active Ingredient
Benzalkonium Chloride 0.13% v/v. Purpose: Antiseptic
Renew Antibacterial Hand Wipes
FDA Label NDC 78899-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kairon Corp. for the product Renew Antibacterial Hand Wipes (NDC 78899-001). 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 - when using, otc - stop use, otc - keep out of reach of children, do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
helps decrease bacteria on the skin
Warnings
Flammable. Keep away from fire or flame. For external use only
Otc - When Using
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if 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.
Do Not Use
on children under 2 months of age or on open skin wounds
Directions
- Adults and children 6 years and older: wet hands thoroughly with product and allow to dry.
- Children under 6 years: should be supervised when using this product.
Other Information
- Store at room temperature and out of direct sunlight. To dispose: place in wastebasket after use. Do not flush.
Inactive Ingredients
aqua, alcohol, glycerin, phenoxyethanol, parfum (fragrance), disodium EDTA, aloe barbadensis leaf juice, tocopheryl acetate, citric acid
Package Label.Principal Display Panel
Package Design Image (Design 01 2)
NDC: 78899 -001-01
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