Otc - Active Ingredient
Active Ingredient Purpose
Benzalkonium Chloride 0.13 percent.............................Antiseptic
Cleanphirst Alcohol Free Antiseptic Hand Sanitizer
FDA Label NDC 52138-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cleanphirst, Llc for the product Cleanphirst Alcohol Free Antiseptic Hand Sanitizer (NDC 52138-100). 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, warnings, dosage & administration, inactive ingredient, 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
Otc - Purpose
Uses
For hand washing to decrease bacteria on the skin.
Recommended for repeated use.
Warnings
Warnings:
For external use only.
Do not use in the eyes.
Discontinue if irritation or redness develop.
If condition persists for more than 72 hours consult a doctor.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Directions: Wet hands thoroughly with product and allow to dry without wiping.
Inactive Ingredient
Inactive Ingredients: Behentrimonium Chloride, Citric Acid, Dihydroxyethyl Cocamine Oxide, Dihydroxpropyl PEG-5, Linoleammonium Chloride, Fragrance, Glycereth-2 Cocoate, Glycerin, Potassium Carbonate, Water.
Package Label.Principal Display Panel
Sanitizerdrugpanel (Cleanphirstsanitizer1)
Cleanphirstsanitizer1 (Cleanphirstsanitizer)
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