Active Ingredient
Benzalkonium chloride 0.1%...........Antiseptic
Antibacterial Wet Wipes
FDA Label NDC 76772-008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tsm Ithalat Ihracat Sanayi Ve Dis Ticaret Limited Sirketi for the product Antibacterial Wet Wipes (NDC 76772-008). 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, keep out of reach of children, do not use, when using this product, stop use and ask a doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Use
decreases bacteria on skin
Warnings
For external use only.
Keep Out Of Reach Of Children
if swallowed
get medical help or contact a Poison Control Center right away.
Do Not Use
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 And Ask A Doctor
if irritation or rash
develops and continues for more than 72 hours
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact
a Poison Control Center right away.
Directions
For adults and children of 2 years and over use
on hands and face to clean and refresh, allow
skin to air dry.
For children under 2 years ask a doctor before use.
Inactive Ingredient
water, propylene glycol,
cocamidopropyl betaine, poly(hexamethyleneguanidine),PEG-7 glyceryl cocoate ,
hydrochloride, glycine, tetrasodium EDTA, tocopheryl acetate, citric acid,
fragrance, methylchloroisothiazolinone, methylisothiazolinone,
PEG-40 hydrogenated castor oil.
* Please review the disclaimer below.
