Active Ingredient
Ethyl Alcohol 66.5%
Instant Hand Sanitizer
FDA Label NDC 50167-7100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Germs Travel, Llc for the product Instant Hand Sanitizer (NDC 50167-7100). 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, for external use only, otc - do not use, otc - stop use, otc - keep out of reach of children, inactive ingredient, 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
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 6 should be supervised while using this product
Inactive Ingredient
Inactive ingredients aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine
Manufactured for GERMS TRAVEL, LLC
Voorhees, NJ 08043 • 877-422-2928 • www.GermsTravel.com
Package Label - Principal Display Panel – Pouch
Instant Hand Sanitizer
Kills 99.99% of germs
Enriched with Aloe Vera
www.GermsTravel.com
0.125 FL. OZ (3.7 ML)
Package Label (PRINCIPAL DISPLAY PANEL – POUCH)
* Please review the disclaimer below.
