Skip to Content

DR. IASO

Medically reviewed on March 2, 2018

Dosage form: cream
Ingredients: OCTINOXATE 7.5g in 100mL
Labeler: IASO Inc
NDC Code: 75847-0002

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 ingredients: water, cyclopentasiloxane, ethylhexyl salicylate, zinc oxide, butylene glycol, dipropylene glycol, glycrrin, peg-10 dimethicone, titanium dioxide, dicaprylyl carbonate, disteardimonium hectorite, magnesium sulfate, dimethicone, calcium aluminum borosilicate, methyl methacrylate crosspolymer, mica, phenoxyethanol, aluminum hydroxide, dimethicone/vinyl dimethicone crosspolymer, aluminum stearate, dimethicone/vinyl dimethicone crosspolymer, aluminum stearate, fragrance, methicone, caprylyl glycol, glyceryl caprylate, microcrystalline cellulose, polyglyceryl-6 polyricinoleate, bambusa vulgaris water, eut6erpe oleracea fruit extract, tocopheryl acetate, vaccinium angustifolium fruit extract, dianthus chinensis extract, nelumbo nucifera flower extract, basil, camellia sinensis, centella asiatica, houttuynia cordata, perilla ocymoides, rosemary, acacia farnesiana, lilium tigrinum, magnolia liliflora, prunus mume, peach, prunus serrulata, thymus quinquecostatus, triethoxycaprylyls, cellulose gum, CI 77492, CI 77491

high level daily sunscreen

keep out of reach of the children

Use before when exposed by the sun

do not use when you feel itching
do not swallow
clean the skin before use

Shake well and apply evenly before sunning
Reapply frequently, and after swimming, perspiring or toweling off

DR. IASO 
octinoxate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75847-0002
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (OCTINOXATE) OCTINOXATE7.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CYCLOMETHICONE 5 
WATER 
OCTISALATE 
ZINC OXIDE 
BUTYLENE GLYCOL 
DIPROPYLENE GLYCOL 
GLYCERIN 
TITANIUM DIOXIDE 
DICAPRYLYL CARBONATE 
HECTORITE 
DIMETHICONE 
MICA 
PHENOXYETHANOL 
ALUMINUM HYDROXIDE 
ALUMINUM STEARATE 
METHICONE (20 CST) 
CAPRYLYL GLYCOL 
GLYCERYL CAPRYLATE 
CELLULOSE, MICROCRYSTALLINE 
BAMBUSA VULGARIS WHOLE 
EUTERPE OLERACEA WHOLE 
.ALPHA.-TOCOPHEROL ACETATE 
LOWBUSH BLUEBERRY 
DIANTHUS CHINENSIS WHOLE 
NELUMBO NUCIFERA FLOWER 
OCIMUM BASILICUM WHOLE 
OOLONG TEA LEAF 
CENTELLA ASIATICA 
HOUTTUYNIA CORDATA WHOLE 
PERILLA FRUTESCENS LEAF 
ROSEMARY 
ACACIA 
LILIUM LANCIFOLIUM WHOLE 
MAGNOLIA LILIIFLORA FLOWER 
PRUNUS MUME FLOWER 
PRUNUS PERSICA FLOWER 
PRUNUS SERRULATA FLOWER 
TRIETHOXYCAPRYLYLSILANE 
CARBOXYMETHYLCELLULOSE SODIUM 
FERRIC OXIDE YELLOW 
FERRIC OXIDE RED 
Packaging
#Item CodePackage Description
1NDC:75847-0002-160 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/17/2012
Labeler - IASO Inc (688771690)
Registrant - IASO Inc (688771690)
Establishment
NameAddressID/FEIOperations
Kolmar Korea Co., Ltd689512611manufacture(75847-0002)

 
IASO Inc

Further information

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

Hide