SOROCI MORNING DRIZZLE BUCKET MIST- witch hazel spray
Onsaemiro 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) Water 49.27%

INACTIVE INGREDIENT

Inactive ingredients: Leontopodium Alpinum Extract, Algae Extract, Aloe Barbadensis Leaf Extract, Biosaccharide Gum-1, Collagen Extract, Butylene Glycol, 1,2-Hexanediol, Betaine, Glycyrrhiza Glabra (Licorice) Root Extract, Prunus Armeniaca (Apricot) Fruit Extract, Coix Lacryma-Jobi Ma-yuen Seed Extract, Propolis Extract, Ulmus Davidiana Root Extract, Portulaca Oleracea Extract, Poncirus Trifoliata Fruit Extract, Lavandula Angustifolia (Lavender) Oil, Sodium Hyaluronate, Linolenic Acid, Sodium Ascorbyl Phosphate

PURPOSE

Purpose: Skin Protectant

WARNINGS

Warnings:

For external use only.

Avoid contact with eyes.

Discontinue use if signs of irritation or rashes appear.

Replace the cap after use.

Keep out of reach of children.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Uses

Uses:

A slightly acidic mist and toner containing carefully selected herbal ingredients such as edelweiss extract for bright and healthy skin.

Directions

Directions:

Spray onto your face with your eyes are closed, use whenever your skin is dry and then gently tap to finish. After cleansing, use instead of Toner. Use before or after makeup.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

SOROCI MORNING DRIZZLE BUCKET MIST
witch hazel spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71498-020
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Witch Hazel (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	Witch Hazel	73.9 g in 150 mL

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
Butylene Glycol (UNII: 3XUS85K0RA)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71498-020-02	1 in 1 CARTON	12/01/2017	07/01/2018
1	NDC:71498-020-01	150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part347	12/01/2017	07/01/2018

Labeler - Onsaemiro Co.,Ltd. (690366048)

Registrant - Onsaemiro Co.,Ltd. (690366048)

Name	Address	ID/FEI	Business Operations
Establishment
EEJE		688222932	manufacture(71498-020)

Revised: 8/2018

Document Id: 96fe3d22-8d52-4ed6-b8b5-11275fa880ff

Set id: 0efa6466-eb21-445f-b9b1-a80dae5fe0a0

Version: 2

Effective Time: 20180822

Onsaemiro Co.,Ltd.