Monarch Hand Sanitizer Gel
FDA Label NDC 63710-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Laboratorios Zeyco, S.a. De C.v. for the product Monarch Hand Sanitizer (NDC 63710-005). 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 drug facts, active ingredient, purpose, use, warnings, do not use, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 70%
Purpose
Antiseptic
Use
for handwashing to decrease bacteria on skin. Recommended for repeated use.
Warnings
For external use only.
Flammable, keep away from fire and flame.
Do Not Use
in the eyes. If this happens, rinse thoroughly with water.
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 swallowed, get medical help or contact a Poison Control Center right away.
Directions
Wet hands thoroughly with product. Rub into skin until dry. Do not wipe off. No rinsing required.
Other Information
Store at no more than 86°F (30°C)
Inactive Ingredients
Aminomethyl propanol, carbomer, glycerin, water.
Package Labeling:500Ml
Bottle (Bottle)
Package Labeling:3.7L
Bottle2 (Bottle2)
Package Labeling: 1L
Bottle3 (Bottle3)
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