Otc - Active Ingredient
Active Ingredient
Benzethonium Chloride 0.095%
Hand Sanitizer
FDA Label NDC 72264-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Biolab International Incorporated for the product Hand Sanitizer (NDC 72264-002). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, dosage & administration, inactive ingredient, storage and handling, indications & usage, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antiseptic
Otc - Keep Out Of Reach Of Children
Keep it out of children.
Dosage & Administration
Directions: Place a small amount of product in your hand, and rub hands together until dry.
Inactive Ingredient
Inactive Ingredients: Water(EAU), Betaine Anhydrous,PEG-40 Hydrogenated Castor Oil, Phenoxyethanol,Diazolidinyl Urea, Palmitamidopropyltrimonium Chloride, Propylene Glycol, Fragrance(Parfum), Sodium Citric Acid, Disodium EDTA.
Storage And Handling
Storage: Avoid direct sunlight.
Indications & Usage
Uses
Decrease bacteria on hands.
Warnings
WarningsFor external use only.
In case of contact with eyes, rinse immediately with plenty of water. Discontinue use if rash or irritation occurs and consult a doctor.
Package Label.Principal Display Panel
Image Of Bottle Label (Lc)
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