MIRACLETOX TIME REWIND ADVANCED ESSENTIAL TONER- niacinamide, adenosine liquid
Beauren Korea Inc.

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, Glycerin, 1,2-Hexanediol, Butylene Glycol, Betaine, PEG-60 Hydrogenated Castor Oil, Sparassis Crispa Extract, Allantoin, Carbomer, Triethanolamine, Hamamelis Virginiana (Witch Hazel) Extract, Disodium EDTA, Fragrance, Centella Asiatica Extract, Sodium Hyaluronate, Scutellaria Baicalensis Root Extract, Bletia Hyacinthina Bulb Extract, Coptis Chinensis Root Extract, Rheum Palmatum Root Extract, Phellodendron Amurense Bark Extract

PURPOSE

Purpose: Skin Brightening & Anti-wrinkle

WARNINGS

Warnings: For external use only. Avoid contact with the eyes. Discontinue use if signs of irritation or rashes appear. Do not use on damaged or broken skin. Close the cap after use.

KEEP OUT OF REACH OF CHILDREN

Keep Out of Reach of Children. Store away from hot or cold places and direct sunlight.

Uses

Uses: Helps skin brightening and anti-wrinkle.

Directions

Directions: After cleansing your face, gently wipe your face with Toner soaked on a cotton pad along the skin texture.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

MIRACLETOX TIME REWIND ADVANCED ESSENTIAL TONER
niacinamide, adenosine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71619-040
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	0.3 g in 15 mL
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.006 g in 15 mL

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71619-040-02	1 in 1 CARTON	08/01/2017	12/31/2020
1	NDC:71619-040-01	15 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		08/01/2017	12/31/2020

Labeler - Beauren Korea Inc. (689700249)

Registrant - Beauren Korea Inc. (689700249)

Name	Address	ID/FEI	Business Operations
Establishment
Dermafirm INC.		690171603	manufacture(71619-040)

Revised: 12/2020

Document Id: b605da3e-99e3-ff9c-e053-2a95a90afb73

Set id: da4a18c0-d0c0-439c-be6b-72546f43d101

Version: 2

Effective Time: 20201209

Beauren Korea Inc.