FDA Label for Hand Sanitizer
View Indications, Usage & Precautions
Hand Sanitizer Product Label
The following document was submitted to the FDA by the labeler of this product Hanover Pen Corp Dba Hpc Global. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Ethyl Alcohol 66.5 percent
Purpose
Antiseptic
Uses
For handwashing to decrease bacteria on skin without soap and water.
Recommended for repeated use.
Warnings
For external use only.
Flammable, keep away from fire or flame.
Do Not Use
Do not use in the eyes, if this happens rinse thoroughly with water.
Stop Use And Ask A Doctor
Stop use and ask a doctor if irritation of redness develops and persists for more than 72 hours.
Keep Out Of Reach Of Children
If ingested get medical help or contact a Poison Control Center right away.
Directions
wet hands throughly with product
allow to dry without wiping
children under six should be supervised while using this product.
Inactive Ingredients
aloe vera, carbomer, D and C number 5, D and C yellow number 10, fragrance, purified water, triethanolamine
Package Label Principal Display Panel
Front Label
NDC 51811-374-14
Hand Sanitizer - Fresh
4 FL OZ (118ML)
Back Label(Drug Facts)
Hand Sanitizer - Fresh
Distributed by
HPC Global, Hanover PA, 17331
Made in USA
* Please review the disclaimer below.