Active Ingredient
Benzalkonium chloride 0.1%
Cb Alcohol Wipes
FDA Label NDC 73529-352
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nutritech Pharmaceuticals, Inc for the product Cb Alcohol Wipes (NDC 73529-352). 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, directions, warnings, otc - keep out of reach of children, inactive ingredients, package label.principal display panel, 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
Directions
For adults and children of 2 years and over.
Children under 2 years ask a doctor before use.
Allow to dry without wiping.
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,avoid contact with eyes and face.
If contact occurs,flush thoroughly with water.
Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact aPoisonControlCenter right away.
Inactive Ingredients
water,sodium lauryl sulfate,fragrance,2-bromo-2-nitropropane-1,3-diol,aloe barbadensis leaf extract,disodium EDTA,trithanolamine ,glycerin,tocopheryl acetate
Package Label.Principal Display Panel
Cb Alcohol Wipes (Wipes)
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