FROM THE SKIN GLUTATHIONE COLLAGEN SUN GEL PATCH- methylene bis-benzotriazolyl tetramethylbutylphenol liquid 
CNP KOREA Co.,Ltd

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Drug Facts

Methylene Bis-Benzotriazolyl Tetramethylbutylphenol

Water
Polyvinyl Alcohol
Glycerin
Glycereth-26
Phenyl Trimethicone
Butylene Glycol
Hydroxyethyl Urea
Dipropylene Glycol
Hydroxyacetophenone
1,2-Hexanediol
Glutathione
Methylene Bis-Benzotriazolyl Tetramethylbutylphenol
Acrylates/C10-30 Alkyl Acrylate Crosspolymer
Arginine
Polyglyceryl-10 Myristate
Polyglyceryl-10 Stearate
Panthenol
Fragrance
Sodium Acetate
Hydrogenated Lecithin
Caprylyl Glycol
Disodium EDTA
Decyl Glucoside
Collagen Extract
Cynanchum Atratum Extract
Porphyra Umbilicalis Extract
Xanthan Gum
Lactobacillus Ferment Lysate
Leontopodium Alpinum Callus Culture Extract
Ocimum Basilicum (Basil) Seed Extract
Panax Ginseng Extract
Saccharomyces Ferment Filtrate
Ethylhexylglycerin
Glucuronic Acid
Tripeptide-29

Transparent Sun Patch:
Provides effective UVA and
UVB protection, applying
seamlessly like a gel to create
an invisible, residue-free film.
Customize application size
& area for tailored coverage,
ideal for those seeking
enhanced sun protection.

keep out of reach of the children

Apply product evenly to the desired areas needing sun protection.

The gel formulation solidifies into a transparent film that can be peeled off after outdoor activities.

Consult a professional if redness, swelling, itching or other abnormal reactions occur during or after use.

Avoid using on wounded areas. Handle with care during storage.
Keep out of reach of children.

Store away from direct sunlight. Avoid contact with the eyes.

topical use only

label

FROM THE SKIN GLUTATHIONE COLLAGEN SUN GEL PATCH 
methylene bis-benzotriazolyl tetramethylbutylphenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84358-0002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BISOCTRIZOLE (UNII: 8NT850T0YS) (BISOCTRIZOLE - UNII:8NT850T0YS) BISOCTRIZOLE0.1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:84358-0002-120 mL in 1 TUBE; Type 0: Not a Combination Product06/02/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02006/02/2024
Labeler - CNP KOREA Co.,Ltd (695103367)
Registrant - CNP KOREA Co.,Ltd (695103367)
Establishment
NameAddressID/FEIBusiness Operations
CNP KOREA Co.,Ltd695103367manufacture(84358-0002)

Revised: 6/2024
Document Id: 19f64b8e-784c-ef18-e063-6394a90ace68
Set id: 19e57332-7ea8-0de0-e063-6294a90a7ed0
Version: 2
Effective Time: 20240603
 
CNP KOREA Co.,Ltd