IUNIK CENTELLA CALMING DAILY SUNSCREEN- diethylamino hydroxybenzoyl hexyl benzoate, ethylhexyl triazone, methylene bis-benzotriazolyl tetramethylbutylphenol cream 
IUNIK 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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​YEGREENA - 43
83403-001_iUNIK Centella Calming Daily Sunscreen

Diethylamino Hydroxybenzoyl Hexyl Benzoate 5%

Ethylhexyl Triazone 4%

Methylene Bis-Benzotriazolyl Tetramethylbutylphenol 2%

Sunscreen

Helps prevent sunburn

Apply liberally 15 minutes before sun exposure. Reapply at least every two hours


Sun protection measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 of higher and other sun protection measures including: 1) Limited time in the sun, especially from 10 am to 2 pm. 2) Wear long-sleeve shirts, pants, hats, and sunglasses

Ask a doctor to use for children under 6 months

For external use only

Do not use on damaged or broken skin

Stop using and ask a doctor if rash occurs

When using this product, keep out of eyes. Rinse with water to remove

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away

Centella Asiatica Extract, Water, Dibutyl Adipate, Glycerin, Niacinamide, Polymethyl Methacrylate, Polysilicone-15, 1,2-Hexanediol, Beta-Glucan, Allantoin, Butylene Glycol, Pentylene Glycol, Arachidyl Alcohol, Sodium Stearoyl Glutamate, Polyglyceryl-3 Methylglucose Distearate, Sorbitan Sesquioleate, Behenyl Alcohol, Decyl Glucoside, Caprylyl Glycol, Arachidyl Glucoside, Hydroxyacetophenone, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Carbomer, Polyacrylate Crosspolymer-6, Adenosine, Dipotassium Glycyrrhizate, Glucose, t-Butyl Alcohol, Xanthan Gum, Tromethamine, Disodium EDTA

image description

IUNIK CENTELLA CALMING DAILY SUNSCREEN 
diethylamino hydroxybenzoyl hexyl benzoate, ethylhexyl triazone, methylene bis-benzotriazolyl tetramethylbutylphenol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83403-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20) (DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE - UNII:ANQ870JD20) DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE5 g  in 100 mL
ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4) (DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE - UNII:ANQ870JD20) ETHYLHEXYL TRIAZONE4 g  in 100 mL
BISOCTRIZOLE (UNII: 8NT850T0YS) (BISOCTRIZOLE - UNII:8NT850T0YS) BISOCTRIZOLE2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
NIACINAMIDE (UNII: 25X51I8RD4)  
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)  
POLYSILICONE-15 (UNII: F8DRP5BB29)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
ALLANTOIN (UNII: 344S277G0Z)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE (UNII: W19EIO0DBE)  
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
DOCOSANOL (UNII: 9G1OE216XY)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
ADENOSINE (UNII: K72T3FS567)  
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)  
XANTHAN GUM (UNII: TTV12P4NEE)  
TROMETHAMINE (UNII: 023C2WHX2V)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
WATER (UNII: 059QF0KO0R)  
DIBUTYL ADIPATE (UNII: F4K100DXP3)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83403-001-021 in 1 CARTON04/18/2023
1NDC:83403-001-0160 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/18/202301/01/2024
Labeler - IUNIK Co., Ltd. (695653625)
Registrant - IUNIK Co., Ltd. (695653625)
Establishment
NameAddressID/FEIBusiness Operations
YEGREENA CO.,LTD.695951904manufacture(83403-001)

Revised: 1/2024
 
IUNIK Co., Ltd.