Active Ingredient
Ethyl Alcohol 70 percent
Hydrating Instant Hand Sanitizer
FDA Label NDC 59371-6510
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Micrylium Laboratories for the product Hydrating Instant Hand Sanitizer (NDC 59371-6510). 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, 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
Antimicrobial
Uses
Cleansing gel for hands that need frequent care.
Decrease bacteria on skin.
Warnings
For external use only.
Flammable, keep away from fire or flame.
Otc - Do Not Use
Do not use in or near the eyes, in case of exposure rinse eyes throughly with water.
Do not use if you have preexisting rash condition.
Otc - Stop Use
Stop use and ask a doctor if irritation, redness or rash appear.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed get medical help or contact Poison Control Center right away.
Directions
Apply approximately 3ml on palm and rub hands for 30 seconds.
Rinsing is not required.
Inactive Ingredients
aloe barbadensis, aroma, blue 1 (CI 42090), carbomer, cetyl alcohol, glycerin, panthenol, tocopherol acetate, triethanolamine, water, yellow 5 (CI 19140)
Package Label.Principal Display Panel
Drug Facts
Monarch Hs 2 Label (Monarch2hs)
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