Active Ingredient
Ethyl Alcohol 63%
Anti-bacterial Hand Sanitizer Gel
FDA Label NDC 72707-029
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 Anti-bacterial Hand Sanitizer (NDC 72707-029). 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 active ingredient, purpose, uses, warnings, when using this product, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
To help reduce bacteria on hands.
Warnings
- For external use only.
- Flammable, keep away from fire, flame and direct sunlight.
When Using This Product
- Avoid contact with eyes and lips.
- If contact occurs, rinse with water.
Otc - Stop Use
Stop use and ask a doctor if 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.
Directions
- Place enough to cover both hands in the palm, and rub hands together until dry.
- Children under 6 years of age should be supervised by adults when applying this product.
Inactive Ingredients:
aminomethyl propanol, carbomer, denatonium benzoate, glycerin, propylene glycol, water.
Package Label.Principal Display Panel
Image Of Bottle Label (Wtg)
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