Active Ingredient
Ethyl Alcohol 66.5 percent
Hand Sanitizer
FDA Label NDC 51811-374
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hanover Pen Corp Dba Hpc Global for the product Hand Sanitizer (NDC 51811-374). 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, do not use, stop use and ask a doctor, 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
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
Image Drug Facts Label (Drugfacts37414)
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