Active Ingredient
Ethyl Alcohol 66.5%
Instant Hand Sanitizer
FDA Label NDC 50225-355
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Global Protection Usa, Inc. for the product Instant Hand Sanitizer (NDC 50225-355). 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, otc - do not use, otc - stop use, 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
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
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
Distributed by
Global Protection USA, Inc.
West Berlin, NJ 08091
800-957-8955
Package Label - Principal Display Panel – Bottle
Global Protection, Inc. “Provider of Homeland Security Equipment”
Instant Hand Sanitizer
Kills 99.9% of Germs
Enriched with Aloe Vera
2 Fl. oz. (59ML)
Package Label (PRINCIPAL DISPLAY PANEL – BOTTLE)
* Please review the disclaimer below.
