MEFACORY SUPER DEEP CLEANSING FOA M- witch hazel cream
MeFactory Co., Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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ACTIVE INGREDIENT

Active ingredients: Hamamelis Virginiana (Witch Hazel) Leaf Extract 0.001%

INACTIVE INGREDIENT

Inactive ingredients: Water, Stearic Acid, Glycerin, Lauric Acid, Potassium Hydroxide, Myristic Acid, Beeswax, Polysorbate 20, Glycol Stearate, 1,2-Hexanediol, Cocamidopropyl Betaine, PEG-100 Stearate, Glyceryl Stearate, Hydroxyacetophenone, Hexylene Glycol, Ethylhexyl Methoxycinnamate , Fragrance, Disodium EDTA, Butylene Glycol, Pentylene Glycol, Illite, Kaolin, CI 14700 , Citrus Paradisi (Grapefruit) Fruit Extract, Citrus Limon (Lemon) Fruit Extract, CI 19140

PURPOSE

Purpose: Skin Protectant

WARNINGS

Warnings: For external use only 1. Discontinue use immediately and consult a dermatologist, if you experience the following: 1) Irritation, red spot, itchy skin or rash 2) Applied skin area has the above reaction from direct sun. 2. Do not use on irritated skin, cuts, or other infected skin areas. 3. Avoid direct contact with eyes

KEEP OUT OF REACH OF CHILDREN

Uses

Uses: Skin cleansing

Directions

Directions: 1. Wet your face with water 2. Apply foaming cleanser into the palms of your hands 3.Rub hands together with water to make bubble 4. Apply the bubble to your face by rubbing your hands on your entire face 5. Wash off the cleanser thoroughly with warm water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of tube

MEFACORY SUPER DEEP CLEANSING FOA M
witch hazel cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70908-170
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Witch Hazel (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	Witch Hazel	0.001 g in 120 g

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:70908-170-01	120 g in 1 TUBE; Type 0: Not a Combination Product	12/01/2017	12/31/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part347	12/01/2017	12/31/2017

Labeler - MeFactory Co., Ltd. (689840967)

Registrant - MeFactory Co., Ltd. (689840967)

Name	Address	ID/FEI	Business Operations
Establishment
CNF CO.,LTD.		689852175	manufacture(70908-170)

Revised: 1/2018

Document Id: 2747f731-ba1f-44fd-b782-b792de351ba2

Set id: be3fd1cd-5752-4b0f-a356-22b053a55851

Version: 2

Effective Time: 20180102

MeFactory Co., Ltd.