Warning
FOR EXTERNAL USE ONLY
Refreshed Traveler Hand Sanitizer
FDA Label NDC 72920-2011
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hand Sanitizer for the product Refreshed Traveler Hand Sanitizer (NDC 72920-2011). 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 warning, active ingredients, otc - keep out of reach of children, otc - stop use, otc - purpose, directions, inactive ingredient, otc - when using, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Ethyl Alcohol
Otc - Keep Out Of Reach Of Children
Do not ingest - If swallowed get medical help or contact a poison control center immediately
Otc - Stop Use
Stop and contact a physician if irritation, redness, or rash develops and persist for longer than 72 hours
Otc - Purpose
Antiseptic to decrease bacteria on the skin
Directions
Throughly apply product on hands and rub together until dry. Adult supervision recommended for anyone under 6 years of age.
Inactive Ingredient
Water, Glycerin, Proptlene Glycol, Fragrance, Acrylates/C10-30 alkyl acrylate crosspolymer, Aminomethyl Propanol, Lactose, Microcrystalline Cellulose, Sucrose, Zea Mays (corn) Starch, Tocopheryl Acetate, Hydroxypropyl, Methylcellulose, Ultramarines (C177007), Maltodextrin, Aloe Barbadensis Leaf Juice, Vitamin E
Otc - When Using
Hand sanitizer to decrease bacteria on the skin
Indications & Usage
Hand sanitizer to decrease bacteria on the hands
* Please review the disclaimer below.
