Active Ingredient:
Ethyl Alcohol 70%
Instant Hand Sanitizer
FDA Label NDC 72180-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Novelty Creative Solutions, Inc. for the product Instant Hand Sanitizer (NDC 72180-101). 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, use, warnings:, keep out of reach of children, 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
Purpose
Antiseptic
Use
Decrease bacteria on hands.
Warnings:
For external use only. Flammable. Keep away from fire or flame. Stop use and ask a doctor if irritation or rash appears or lasts.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a doctor right away.
Directions
Pump as needed into your hands. Rub until hands are dry. Children under 6yr. old should be supervised when using this product.
Other Information:
Store below 118°F.
Inactive Ingredients:
Water(Aqua), Propylene Glycol, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance, Fragrance(Parfum), Aloe Barbadensis Leaf Juice, Denatonium Benzoate, Maltodextrin, Tocopheryl Acetate.
Package Label.Principal Display Panel
Image Of Bottle Label (30ml)
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