FDA Label for Koi Hand Sanitizer
View Indications, Usage & Precautions
Koi Hand Sanitizer Product Label
The following document was submitted to the FDA by the labeler of this product Koi Cbd Llc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Ethyl Alcohol 62%...... Antimicrobial
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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