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Dr.eslee Sun Matte

Dosage form: liquid
Ingredients: OCTINOXATE 7.5g in 100g
Labeler: Ajou Medics Co., Ltd
NDC Code: 76340-3001

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.

Drug Facts

active ingredient:  ethylhexyl methoxycinnamate

inactive ingredient:  Butylene Glycol, 4-Methylbenzylidene Camphor, Titanium Dioxide, Cetyl Alcohol, Octocrylene, Hydrogenated Polydecene, Polysorbate 80, Cyclomethicone, Stearic Acid, Glyceryl Stearate, PEG-100 Stearate, Sorbitan Stearate, Polyhydroxystearic Acid, Aluminum Hydroxide, Triethanolamine, Carbomer, Xanthan Gum, Poncirus Trifoliata Fruit Extract, Aloe Barbadensis Leaf Juice, Sodium Hyaluronate, Biosaccharide Gum-1, Tocopheryl Acetate, Disodium EDTA, Salicylic Acid, Farnesyl Acetate, Farnesol, Panthenyl, Triacetate, Hydrolyzed Algin, Zinc Sulfate, Phenoxyethanol, Methylparaben, Propylparaben, Butylparaben

helps protect from UV-Rays

keep out of reach of the children

■ Apply Proper Amount of the cream on skin before sun exposure.

■ For external use only. Avoid contact with eyes.
■ Avoid contact with eyes.
■ Do not swallow. If swallowed, get medical help.
■ Keep out of reach of children.
■ Stop use and ask doctor if rash and irritation develops.

■ Reapply Frequently, every 2 hours for best result

DR.ESLEE SUN MATTE 
octinoxate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76340-3001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (OCTINOXATE) OCTINOXATE7.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
BUTYLENE GLYCOL 
ENZACAMENE 
TITANIUM DIOXIDE 
C12-16 ALCOHOLS 
OCTOCRYLENE 
HYDROGENATED POLYDECENE (550 MW) 
POLYSORBATE 80 
CYCLOMETHICONE 
STEARIC ACID 
GLYCERYL MONOSTEARATE 
PEG-100 STEARATE 
SORBITAN MONOSTEARATE 
POLYHYDROXYSTEARIC ACID (2300 MW) 
ALUMINUM HYDROXIDE 
TROLAMINE 
XANTHAN GUM 
ALOE VERA LEAF 
HYALURONATE SODIUM 
BIOSACCHARIDE GUM-1 
EDETATE DISODIUM 
SALICYLIC ACID 
FARNESOL 
ZINC SULFATE 
PHENOXYETHANOL 
METHYLPARABEN 
PROPYLPARABEN 
BUTYLPARABEN 
Packaging
#Item CodePackage Description
1NDC:76340-3001-160 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/10/2011
Labeler - Ajou Medics Co., Ltd (688796473)
Registrant - Ajou Medics Co., Ltd (688796473)
Establishment
NameAddressID/FEIOperations
Ajou Medics Co., Ltd688796473manufacture

Revised: 08/2011
 
Ajou Medics Co., Ltd

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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