AOMI HAND SANITIZER- alcohol spray

AOMI HAND SANITIZER by

Drug Labeling and Warnings

AOMI HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Mirfeel Korea Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ALCOHOL 70.0% (w/w)

INACTIVE INGREDIENT

Water, Glycerin, Fragrance, Cymbopogon Citratus Extract, Anthemis Nobilis Flower Extract, Aspalathus Linearis Extract, Melaleuca Alternifolia(Tea Tree)Leaf Extract

PURPOSE

ANTISEPTIC

WARNINGS

For external use only. Flammable. Keep away from heat or flame
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Do not use
in children less than 2 months of age
on open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Hand sanitizer to help reduce bacteria that potentially can cause disease.

Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

QUESTIONS

www.mirfeel.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AOMI HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75010-040
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	Alcohol	70 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75010-040-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2020

Labeler - Mirfeel Korea Co., Ltd (695004258)

Registrant - Mirfeel Korea Co., Ltd (695004258)

Establishment
Name	Address	ID/FEI	Business Operations
Mirfeel Korea Co., Ltd		695004258	manufacture(75010-040)