KOI HAND SANITIZER- ethyl alcohol, 62% gel

Koi Hand Sanitizer by

Drug Labeling and Warnings

Koi Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Koi CBD LLC, Brad Ridenour. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 62%...... Antimicrobial

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.

DO NOT USE

Do not use in eyes. In case of contact, rinse thoroughly with water.

STOP USE

Stop use and consult a doctor if irritation and redness develop and persist for more than 72 hours.

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.

PRINCIPAL DISPLAY PANEL

59 mL NDC: 73842-002-01

INGREDIENTS AND APPEARANCE

KOI HAND SANITIZER 
ethyl alcohol, 62% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73842-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PANTHENOL (UNII: WV9CM0O67Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73842-002-01	59 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/13/2020

Labeler - Koi CBD LLC (072518336)

Registrant - Brad Ridenour (072518336)

Establishment
Name	Address	ID/FEI	Business Operations
Koi CBD LLC		072518336	manufacture(73842-002)