DR.ESLEE SUN PROTECTION- octinoxate cream 
Ajou Medics 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.

----------

Drug Facts

active ingredient: ethylhexyl methoxycinnamate

inactive ingredient: Water, Propylene Glycol, Cyclopentasiloxane, Ethylhexyl Salicylate, Zinc Oxide,
Cyclohexasiloxane, Titanium Dioxide, Cetyl PEG/PPG-10/1 Dimethicone, Hydrogenated Poly(C6-14 Olefin), Betaine, Isoamyl p-Methoxycinnamate, Dimethicone, Disteardimonium Hectorite, Magnesium Sulfate, Methyl Methacrylate Crosspolymer, Silica, imethicone/Vinyl Dimethicone Crosspolymer, Aluminum Hydroxide, Stearic Acid, Triethoxycaprylylsilane, Tocopheryl Acetate, Houttuynia Cordata Extract, Allantoin, Hydrolyzed Collagen, Biosaccharide Gum-1, Portulaca Oleracea Extract, Phenoxyethanol, Methylparaben , Propylparaben, Butylparaben, Fragrance

helps to protect from UV-Rays

keep out of reach of the children

apply proper amount of the cream on the skin before sun exposure

■ For external use only.
■ 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.

apply frequently every 2 hours for best result

package label
DR.ESLEE SUN PROTECTION 
octinoxate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76340-0004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
BETAINE (UNII: 3SCV180C9W)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
METHYL METHACRYLATE (UNII: 196OC77688)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ALGELDRATE (UNII: 03J11K103C)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)  
ALLANTOIN (UNII: 344S277G0Z)  
BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)  
PURSLANE (UNII: M6S840WXG5)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76340-0004-160 g in 1 TUBE; Type 0: Not a Combination Product03/11/201804/18/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/11/201804/18/2022
Labeler - Ajou Medics Co., Ltd (688796473)
Registrant - Ajou Medics Co., Ltd (688796473)
Establishment
NameAddressID/FEIBusiness Operations
Ajou Medics Co., Ltd688796473manufacture(76340-0004)

Revised: 4/2022
 
Ajou Medics Co., Ltd