Otc - Active Ingredient
Active Ingredients:
Ethanol 62%
Hand Sanitizer
FDA Label NDC 73326-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jacent Strategic Merchandising, Llc. for the product Hand Sanitizer (NDC 73326-001). 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, indications & usage, warnings, otc - stop use, otc - keep out of reach of children, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antiseptic
Indications & Usage
Use
To decrease bacteria on the skin .
Warnings
Warnings
Flammable. Keep away from fire or flame.
For external use only.
Do not use in the eyes.
Otc - Stop Use
Discontinue use if irritation or redness develop. If condition persists for more that 72 hours, consult a doctor.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Directions
Rub into skin until dry.
Inactive Ingredient
Inactive ingredients
Water, Aloe Barbadensis Leaf Juice, Maltodextrin, Vitamin E, Glycerin, Propylene Glycol, Fragrance, Acrylates/C10-C30 alkyl acrylate crosspolymer, Triethanolamine.
Other Safety Information
Other Information
Store below 110F. Avoid direct sunlight, fluorescent lightning,heat and moisture.
Package Label.Principal Display Panel
Image Of Bottle Label (Hd2)
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