IOPE S.S. CONDITIONING COLOR BASE No.40 SPF22 PA PLUS

Dosage form: lotion
Ingredients: Octinoxate 0.05mL in 1mL, TITANIUM DIOXIDE 0.0439mL in 1mL, ZINC OXIDE 0.0098mL in 1mL
Labeler: AMOREPACIFIC
NDC Code: 43419-354

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

IOPE
S.S CONDITIONING
COLOR BASE
[SPF 22/PA+]

WARNING LABEL

FOR EXTERNAL USE ONLY. AVOID CONTACT WITH EYES.

DISCONTINUE USE IF SIGNS OF IRRITATION APPEAR,

KEEP OUT OF REACH OF CHILDREN

ACTIVE INGREDIENTS

ETHYLHEXYL METHOXYCINNAMATE 5.0%, TITANIUM DIOXIDE 4.39%, ZINC OXIDE 0.98%

INGREDIENTS

WATER, CYCLOPENTASILOXANE, PROPANEDIOL, ETHYLHEXYL METHOXYCINNAMATE, PHENYL TRIMETHICONE, TITANIUM DIOXIDE, POLYMETHYL METHACRYLATE, SQUALANE, DICAPRYLYL CARBONATE, CETYL PEG/PPG-10/1 DIMETHICONE, DISTEARDIMONIUM HECTORITE, SORBITAN ISOSTEARATE, OZOKERITE, CAMELLIA SINENSIS LEAF EXTRACT, SODIUM CHLORIDE, SILICA, ZINC OXIDE, BETA-GLUCAN, CYCLOHEXASILOXANE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, CALCIUM STEARATE, MICROCRYSTALLINE WAX, SORBITAN SESQUIOLEATE, ALUMINUM HYDROXIDE, STEARIC ACID, GLYCERIN, CHROMIUM OXIDE GREENS, CAPRYLYL GLYCOL, TRIETHOXYCAPRYLYLSILANE, DISODIUM EDTA, LAVANDULA STOECHAS EXTRACT, ETHYLHEXYLGLYCERIN, BORON NITRIDE, MINERAL WATER, IRON OXIDE (CI77492), PHENOXYETHANOL, METHYLPARABEN, HYDROXYPROPYL BISPALMITAMIDE MEA, ETHYL PARABEN, BUTYLPARABEN, ISOBUTYLPARABEN, PROPYLPARABEN, POLYGLUTAMIC ACID, CHLORPHENESIN, FRAGRANCE

PRINCIPAL DISPLAY PANEL - 40 Carton

IOPE

IOPE

SMALL&SMOOTH

S.S CONDITIONING
COLOR BASE

PRINCIPAL DISPLAY PANEL - 60 Carton

IOPE

IOPE

SMALL&SMOOTH

S.S CONDITIONING
COLOR BASE

IOPE S.S. CONDITIONING COLOR BASE NO.40  SPF22 PA PLUS
octinoxate, titanium dioxide, and zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43419-354
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Octinoxate (Octinoxate) Octinoxate0.05 mL  in 1 mL
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE0.0439 mL  in 1 mL
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE0.0098 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CYCLOMETHICONE 5 
PROPANEDIOL 
PHENYL TRIMETHICONE 
SQUALANE 
DICAPRYLYL CARBONATE 
GREEN TEA LEAF 
SODIUM CHLORIDE 
SILICON DIOXIDE 
CYCLOMETHICONE 6 
CALCIUM STEARATE 
MICROCRYSTALLINE WAX 
SORBITAN SESQUIOLEATE 
ALUMINUM HYDROXIDE 
STEARIC ACID 
CHROMIC OXIDE 
CAPRYLYL GLYCOL 
EDETATE DISODIUM 
ETHYLHEXYLGLYCERIN 
PHENOXYETHANOL 
METHYLPARABEN 
ETHYLPARABEN 
BUTYLPARABEN 
ISOBUTYLPARABEN 
PROPYLPARABEN 
CHLORPHENESIN 
Packaging
#Item CodePackage Description
1NDC:43419-354-0135 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35211/01/2010
IOPE S.S. CONDITIONING COLOR BASE NO.60  SPF22 PA PLUS
octinoxate, titanium dioxide, and zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43419-355
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Octinoxate (Octinoxate) Octinoxate0.05 mL  in 1 mL
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE0.0439 mL  in 1 mL
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE0.0098 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CYCLOMETHICONE 5 
PROPANEDIOL 
PHENYL TRIMETHICONE 
SQUALANE 
DICAPRYLYL CARBONATE 
GREEN TEA LEAF 
SODIUM CHLORIDE 
SILICON DIOXIDE 
CYCLOMETHICONE 6 
CALCIUM STEARATE 
MICROCRYSTALLINE WAX 
SORBITAN SESQUIOLEATE 
ALUMINUM HYDROXIDE 
STEARIC ACID 
CHROMIC OXIDE 
CAPRYLYL GLYCOL 
EDETATE DISODIUM 
ETHYLHEXYLGLYCERIN 
PHENOXYETHANOL 
METHYLPARABEN 
ETHYLPARABEN 
BUTYLPARABEN 
ISOBUTYLPARABEN 
PROPYLPARABEN 
CHLORPHENESIN 
Packaging
#Item CodePackage Description
1NDC:43419-355-0235 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35211/01/2010
Labeler - AMOREPACIFIC (687995683)
Establishment
NameAddressID/FEIOperations
AMOREPACIFIC687995683MANUFACTURE

Revised: 10/2010
 
AMOREPACIFIC

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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