Active Ingredient
Benzalkonium Chloride 0.1%
Personal Care
FDA Label NDC 72133-431
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Delta Brands & Products, Llc for the product Personal Care (NDC 72133-431). 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 and ask a doctor if, 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
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
adults and children 2 years and over ■ apply to hands
■ allow to dry without wiping.
children under 2 years ask a doctor before use.
Inactive Ingredients
water, propylene glycol, cocamidopropyl betaine, PEG-7 glyceryl cocoate, fragrance, benzyl alcohol, methylchloroisothiazolinine, methylisothiazolinone, PEG-40 hydrogenated castor oil, tetrasodium EDTA, cetrimonium chloride, citric acid, tocopherol acetate
Package Label
Package Label (Prsnlcreantibacwpes)
* Please review the disclaimer below.
