Active Ingredient
Benzalkonium Chloride 0.1%
Wet Wipes
FDA Label NDC 70140-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Gulsah Uretim Pazarlama - Husey In Kaya for the product Wet Wipes (NDC 70140-001). 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, uses, warnings, do not use, when using this product, stop use, 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
Antiseptic
Uses
•decreases bacteria on the skin
Warnings
•For external use only
Do Not Use
•Over large areas of the body if you are allergic to any of the ingredients
When Using This Product
•do not get into eyes. •If contact occurs, rinse thoroughly with water.
Stop Use
Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours
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
• for adults and children 2 years and over use on hands and face to clean and refresh, allow skin to air dry. For children under 2 years of age ask a doctor before use.
Inactive Ingredients
water, propylene glycol, cocamidopropyl betaine, peg-7 glyceryl cocoate, fragrance, benzyl alcohol, methylchloroisothiazolinine, methylisothiazolinone, tetrasodium EDTA, peg-40 hydrogenated castor oil, cetrimonium chloride, citric acid, aloe vera extract, alphatocopherol acetate
Package Label
Package Label (Bzkclwpelbl)
* Please review the disclaimer below.
