Otc - Active Ingredient
Ethyl Alcohol 62%...... Antimicrobial
Koi Hand Sanitizer
FDA Label NDC 73842-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Koi Cbd Llc for the product Koi Hand Sanitizer (NDC 73842-002). 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, indications & usage, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antimicrobial
Indications & Usage
Hand sanitizer to help decrease bacteria on the skin. Recommended for repeat use.
Warnings
For external use only. Flammable, keep away from fire or flames.
Otc - Do Not Use
Do not use in eyes. In case of contact, rinse thoroughly with water.
Otc - Stop Use
Stop use and consult a doctor if irritation and redness develop and persist for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Dosage & Administration
Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.
Storage And Handling
Do not store about 110°F. Harmful to wood finishes and plastics.
Inactive Ingredient
Deionized Water, Glycerin, Propylene Glycol, Organic Aloe Barbadensis (Aloe Vera) Leaf Extract, Panthenol (Pro-Vitamin B5), Tocopheryl Acetate (Vitamin E Acetate), Carbomer, Aminomethyl Propanol, Fragrance.
Package Label.Principal Display Panel
59 mL NDC: 73842-002-01
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