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FASCY LAB GREEN PLUS SUN

Medically reviewed by Drugs.com. Last updated on Apr 15, 2020.

Dosage form: cream
Ingredients: DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE 1.0g in 50mL, BEMOTRIZINOL 0.5g in 50mL
Labeler: FASCY Co,.LTD.
NDC Code: 70991-200

ACTIVE INGREDIENT

Active Ingredient: 

DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE 2.0%
BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE 1.0%

INACTIVE INGREDIENT

Inactive Ingredients:

WATER, BUTYLENE GLYCOL, C12-15 ALKYL BENZOATE, METHYL METHACRYLATE CROSSPOLYMER, 1,2-HEXANEDIOL, NIACINAMIDE, BEHENYL ALCOHOL, POTASSIUM CETYL PHOSPHATE, SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, POLYISOBUTENE, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER, SILICA, ADENOSINE, CAPRYLYL/CAPRYL GLUCOSIDE, DISODIUM EDTA, SORBITAN OLEATE, SODIUM HYALURONATE

PURPOSE

Purpose: Sunscreen

WARNINGS

Warnings: 

1) In case of any abnormal symptoms or side effects such as redness, swelling or itching during and after use, consult a specialist.
2) Avoid using in injured areas.
3) Storage and handling cautions: a) keep away from children, b) keep away from direct sunlight.
4) For external use only

KEEP OUT OF REACH OF CHILDREN

keep away from children

Uses

Uses
Helps prevent sunburn.

Directions

Directions
Apply thoroughly on parts of your skin exposed to the sun.
Reapply often (every 2 hours) and after swimming, excessive perspiration and washing to ensure maximum sun protection.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FASCY LAB GREEN PLUS SUN 
diethylamino hydroxybenzoyl hexyl benzoate, bemotrizinol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70991-200
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE) DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE1.0 g  in 50 mL
BEMOTRIZINOL (BEMOTRIZINOL) BEMOTRIZINOL0.5 g  in 50 mL
Inactive Ingredients
Ingredient NameStrength
Water 
BUTYLENE GLYCOL 
ALKYL (C12-15) BENZOATE 
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER 
1,2-HEXANEDIOL 
NIACINAMIDE 
DOCOSANOL 
POTASSIUM CETYL PHOSPHATE 
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) 
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER 
SILICON DIOXIDE 
ADENOSINE 
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE 
EDETATE DISODIUM ANHYDROUS 
SORBITAN MONOOLEATE 
HYALURONATE SODIUM 
Packaging
#Item CodePackage Description
1NDC:70991-200-021 TUBE in 1 CARTON
1NDC:70991-200-0150 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/01/2020
Labeler - FASCY Co,.LTD. (689204222)
Registrant - FASCY Co,.LTD. (689204222)
Establishment
NameAddressID/FEIOperations
Greencos Co., Ltd.694777325manufacture(70991-200)

 
FASCY Co,.LTD.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.