FORESTHEAL WITCH HAZEL FACIAL TONER- niacinamide, adenosine liquid
BONNE CO.,LTD

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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ACTIVE INGREDIENT

Active ingredients: NIACINAMIDE 2.0%, ADENOSINE 0.04%

INACTIVE INGREDIENT

Inactive ingredients:

Water, Dipropylene Glycol, Butylene Glycol, Glycerin, Alcohol Denat., Styrene/Acrylates Copolymer, Sodium Citrate, Dipotassium Glycyrrhizate, Citric Acid, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Rosa Centifolia Flower Water, Aloe Barbadensis Leaf Water, Hamamelis Virginiana (Witch Hazel) Water, Carapa Guaianensis Seed Oil, 1,2-Hexanediol, Alcohol, Coix Lacryma-Jobi Ma-yuen Seed Extract, Ethylhexylglycerin, Camellia Sinensis Leaf Extract, Phenoxyethanol, Chlorphenesin, Fragrance

PURPOSE

Purpose: Skin Brightening, Anti wrinkle

WARNINGS

Warnings:

Do not use on damaged or broken skin

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

Keep Out of Reach of Children

KEEP OUT OF REACH OF CHILDREN

Uses

Uses:

Helps brighten the skin tone and improve the look of wrinkles.

Directions

Directions:

Apply the appropriate amount by wiping the skin according to the direction of the skin, or absorb by tapping on the entire face after cleansing.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

FORESTHEAL WITCH HAZEL FACIAL TONER
niacinamide, adenosine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69997-180
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	6.0 g in 300 mL
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.12 g in 300 mL

Ingredient Name	Strength
Inactive Ingredients
Water (UNII: 059QF0KO0R)
Dipropylene Glycol (UNII: E107L85C40)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69997-180-02	1 in 1 CARTON	02/01/2018	06/29/2018
1	NDC:69997-180-01	300 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		02/01/2018	06/29/2018

Labeler - BONNE CO.,LTD (557821750)

Registrant - BONNE CO.,LTD (557821750)

Name	Address	ID/FEI	Business Operations
Establishment
whitecospharm		688442259	manufacture(69997-180)

Revised: 7/2018

Document Id: 362fbbbe-4127-4d4c-a5ca-d2cfeeae4424

Set id: 07732474-b269-4567-b608-4865e237e709

Version: 3

Effective Time: 20180710

BONNE CO.,LTD