Active Indgredient
Ethyl Alcohol 70%
Antimicrobial Hand Sanitizer Gel
FDA Label NDC 51811-721
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 Antimicrobial Hand Sanitizer Gel (NDC 51811-721). 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 indgredient, purpose, uses, warnings, otc - do not use, otc - stop use, otc - 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.
- Recommended for repeated use.
Warnings
for external use only.
Flammable, keep away from fire or flame.
Otc - Do Not Use
Do not use in the eyes, if this happens rinse thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
If ingested get medical help or contact a Poison Control Center right away.
Directions
- wet hands thoroughly with product allow to dry without wiping
- children under six should be supervised while using this product.
Inactive Ingredients
aloe vera, carbomer, purified water, triethanolamine
Antimicrobial Hand Sanitizer Gel - Unscented 1.0 fl. oz.
Pkgd by HPC Global, Hanover PA, 17331 Made in USA
Lot# ****
Package Label.Principal Display Panel
Drug Facts
Drug Facts (4721 604)
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