Otc - Active Ingredient
Ethyl Alocohol 62% by wt.
Muse Health Hand Sanitizer
FDA Label NDC 71683-011
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cc Wellness for the product Muse Health Hand Sanitizer (NDC 71683-011). 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 otc - active ingredient, otc - purpose, uses, warnings, when using this product, stop use and ask a doctor, 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
Otc - Purpose
Antiseptic
Uses
To decrease bacteria on the skin that could cause disease.
Recommended for repeated use.
Warnings
For external use only: hands
When Using This Product
Keep out of eyes.
In case of contact with eyes, flush thoroughly with water.
Avoid contact with broken skin.
Do not inhale or ingest.
Stop Use And Ask A Doctor
Irritation and redness develop
Condition persists for more than 72 hours
Otc - 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 and allow to dry without wiping.
For children under 6, use only under adult supervision.
Not recommended for infants.
Other Information
Do not store above 105°
May discolor some fabrics
Harmful to wood finishes and plastics
Inactive Ingredient
Water (Aqua), Glycerin, Tocopheryl Acetate, Isopropyl Palmitate, Acrylates Copolymer, Aminomethyl Propranolol, Parfum
Questions?
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Product Labeling (Picture1)
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