Florance Morris Antiseptic Hand Sanitizer
FDA Label NDC 76612-180
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Asimex International Llc for the product Florance Morris Antiseptic Hand Sanitizer (NDC 76612-180). 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 drug facts, active ingredient, purpose, use, warnings, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl alcohol 80%
Purpose
Antiseptic
Use
■To decrease bacteria on the skin that could cause disease
■Recommended for repeated use
Warnings
For external use only: hands.
■Flammable ■Keep away from fire or flame
When using this product ■Keep out of eyes ■In case of contact with eyes, flush thoroughly with water ■Avoid contact with broken skin ■Do not inhale or ingest
Stop use and ask a doctor if ■Irritation or redness develops. ■Condition persists for more than 72 hours
Directions
Thoroughly cover your hands with product and allow to dry without wiping ■Children under 6 years of age should be supervised when using this product ■Not recommended for infants
Other Information
Store below 105°F ■May discolor some fabrics ■Harmful to wood finishes and plastics
Inactive Ingredients
Cellulosic thickener, Glycerin, Triethanolamine, Water
Packaging
Image Description (Label3.1)
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