BANDHA FOR AND MASK- niacinamide, adenosine patch

BANDHA FOR AND MASK by

Drug Labeling and Warnings

BANDHA FOR AND MASK by is a Otc medication manufactured, distributed, or labeled by DKCOSTECH, HANSCOS Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

NIACINAMIDE 2.0%
ADENOSINE 0.04%

INACTIVE INGREDIENTS

Water, Dendropanax Morbiferus Leaf Extract, Propanediol, Glycerin, 1,2-Hexanediol, Butylene Glycol, betaine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tromethamine, Xanthan Gum, Aloe Barbadensis Leaf Extract, Astragalus Membranaceus Root Extract, Boswellia Serrata Extract, Melia Azadirachta Leaf Extract, Phyllanthus Emblica Extract, Trifolium Pratense (Clover) Flower Extract, Garcinia Cambogia Fruit Extract, Allantoin, Disodium EDTA, Fragrance, Sodium Hyaluronate

PURPOSE

Brightening
Anti-wrinkle

WARNINGS

1. For external use only
2. Avoid contact with eyes.
3. Discontinue use if signs of irritation or rashes appear.
4. Keep out of reach of children.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Uses

■ Helps brighten skin tone.
■ Helps prevent wrinkle problem.

Directions

1. After cleansing your face,
2. Leave it on for 20 minutes.
3. Gently remove the mask and pat the remaining essence into your face.

QUESTIONS

+8227978088
www.bandha.co.kr

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BANDHA FOR AND MASK 
niacinamide, adenosine patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80623-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	0.56 g  in 28 g
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.01 g  in 28 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Propanediol (UNII: 5965N8W85T)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80623-010-02	10 in 1 CARTON	09/01/2020
1	NDC: 80623-010-01	28 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/01/2020

Labeler - DKCOSTECH (695504288)

Registrant - DKCOSTECH (695504288)

Establishment
Name	Address	ID/FEI	Business Operations
HANSCOS Co.,Ltd.		688494423	manufacture(80623-010)