Otc - Active Ingredient
Ethyl Alcohol 70%...... Antimicrobial
Koi Hand Sanitizer
FDA Label NDC 73842-003
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 73842-003). 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 children less than 2 months of age or on open skin wounds.
Otc - Stop Use
Stop use and consult a doctor if irritation or rash occurs. These may be signs of a serious condition.
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.
Storage And Handling
Do not store about 110°F. Harmful to wood finishes and plastics.
Inactive Ingredient
Water, Glycerin, Propylene Glycol,Carbomer, Triethanolamine, Fragrance.
Package Label.Principal Display Panel
NDC 73842-003-001 Bottle 59 mL
2oz-sanitizer-2.jpg (2oz Sanitizer 2)
NDC 73842-003-002 Bottle 118 mL
4oz-sanitizer-2.jpg (4oz Sanitizer 2)
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