KOKU ALL NATURAL HAND BODY 80 PERCENT VEGAN ETHYL ALCOHOL MANDARIN ORANGE- alcohol liquid

Koku All Natural Hand Body 80 Percent Vegan Ethyl Alcohol Mandarin Orange by

Drug Labeling and Warnings

Koku All Natural Hand Body 80 Percent Vegan Ethyl Alcohol Mandarin Orange by is a Otc medication manufactured, distributed, or labeled by H&Y Products LLC dba Kolonya Carre. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl alcohol 80%

Purpose

Antiseptic

Use

for hand washing to decrease bacteria on the skin.

Warnings

For external use only

Flammable, keep away from fire or flame. 

Do not use

• in the eyes

Stop use and ask a doctor if

• irritation and redness develop.
• condition persists for more than 72 hours.

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. 

Inactive ingredients

Water, Fragrance, Benzyl salicylate, Citral, Citronellol, Geraniol, Limonene, Linalool.

Package Labeling: 82127-008-02

Package Labeling: 82127-008-01

INGREDIENTS AND APPEARANCE

KOKU ALL NATURAL HAND BODY 80 PERCENT VEGAN ETHYL ALCOHOL MANDARIN ORANGE 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82127-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.8 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
CITRAL (UNII: T7EU0O9VPP)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
COUMARIN (UNII: A4VZ22K1WT)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
LINALOOL, (+/-)- (UNII: D81QY6I88E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82127-008-02	1 in 1 BOX	09/15/2022	07/31/2025
1		35 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 82127-008-01	1 in 1 BOX	09/15/2022	07/31/2025
2		90 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/15/2022	07/31/2025

Labeler - H&Y Products LLC dba Kolonya Carre (070644433)

Registrant - H&Y Products LLC dba Kolonya Carre (070644433)