Pro Advantage Instant Hand Sanitizer
FDA Label NDC 43128-118
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ndc National Distribution & Contracting, Inc. for the product Pro Advantage Instant Hand Sanitizer (NDC 43128-118). 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 pro advantage instant hand sanitizer gel, active ingredients:, purpose, use, warning:, when using this product, ask a doctor before use if you have, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients:
Alcohol 62%
Purpose
Antiseptic
Use
To help reduce bacteria on the hands that can potentially cause disease.
Warning:
• For External Use Only
• Flammable, keep away from fire or flame.
When Using This Product
• Avoid contact with eyes, if this occurs rinse thoroughly with water and contact a physician.
Ask A Doctor Before Use If You Have
• Deep wounds, animals bites or serious burns.
Stop Use And Ask A Doctor If
• Condition persists.
Keep Out Of Reach Of Children.
• If swallowed get medical help or contact a Poison Control Center right away.
Directions:
Apply a liberal amount to hands and rub hands thoroughly until dry. Do not rinse or wipe off gel.
Inactive Ingredients:
Water, Glycerin, Fragrance, Carbomer, Triethanolamine, DMDM Hydantoin
Ref: P779118 Ndc 43128-118-04
Made in China
www.ProAdvantagebyNDC.com
Manufactured for NDC, Inc.
407 New Sanford Road, La Vergne, TN 37086
Product Labels
Hand Sanitizer Gel Label (Handsanitizergellabel)
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