Otc - Active Ingredient
Active Ingredient:
Benzethonium Chloride 0.095%
Hand Sanitizer
FDA Label NDC 72707-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Disney Destinations,llc for the product Hand Sanitizer (NDC 72707-001). 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, otc - stop use, otc - keep out of reach of children, dosage & administration, inactive ingredient, 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 - Stop Use
Stop using this product and consult a doctor if irritation or redness develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a poison control center immediately.
Dosage & Administration
Directions
- Rub dime sized amount between hands until dry.
- For use by children under 6 years, adult supervision is required.
Inactive Ingredient
Inactive Ingredients
Fragrance, Glycerin, Methylisothiazolinone, PEG-40 Hydrogenated Castor Oil, Polyquatemium-37, Propylene Glycol, Triethanolamine, Water,
Indications & Usage
Uses
To help reduce bacteria on hands.
Warnings
Warnings:
For external use only.
Otc - When Using
When using this product,
- Avoid contact with eyes and lips.
- If contact occurs, rinse with water.
Package Label.Principal Display Panel
Image Of Bottle Label (Disney)
* Please review the disclaimer below.
