BOTOKI V MASK by FICC Co., Ltd. / GEOSEONGGDS

BOTOKI V MASK by

Drug Labeling and Warnings

BOTOKI V MASK by is a Otc medication manufactured, distributed, or labeled by FICC Co., Ltd., GEOSEONGGDS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BOTOKI V MASK- adenosine patch 
FICC 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

ADENOSINE 0.04%

INACTIVE INGREDIENTS

Purified Water, Glycerin, Gelatin, Sodium Polyacrylate, Polyvinyl Alcohol, PVP, Tartaric Acid, Aluminum Hydroxide, Green Tea Extract, Tocopherol, Grape Seed Extract, Collagen, Caffeine, Polysorbate 20, Disodium EDTA, Glaucine, Phosphatidylcholine, Hyaluronic Acid, Urea, Menthol, Perfume, Methionyl r-Clostridium, Botulinum, Polypeptide-1, Hexapeptide-40, Sodium Chloride, Disodium Phosphate, Potassium Phosphate

PURPOSE

Anti wrinkle

WARNINGS

For external use only
Consult a specialist if there are abnormal symptoms or side effects such as redness, swelling or itchiness due to direct sunlight during or after use.
Avoid using on wounded areas.
Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

Uses

■ Helps improve wrinkle problem

Directions

■ Stretch the product sufficiently and adhere to ears.
■ Remove the product after the absorption of thick water gel and massage gently into skin.

Other Information

■ Keep away from direct sunlight.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

BOTOKI V MASK 
adenosine patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 81647-150
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.006 g  in 15 g
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Gelatin (UNII: 2G86QN327L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 81647-150-024 in 1 CARTON07/01/202110/01/2022
1NDC: 81647-150-0115 g in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/01/202110/01/2022
Labeler - FICC Co., Ltd. (695721074)
Registrant - FICC Co., Ltd. (695721074)
Establishment
NameAddressID/FEIBusiness Operations
GEOSEONGGDS695439607manufacture(81647-150)

Revised: 10/2023
 

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