IOPE SS description, usages, side effects, indications, overdosage, supplying and lots more!

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IOPE SS

AMOREPACIFIC

IOPE SMALL&SMOOTH S.S CONDITIONING FOUNDATION


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

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 3.0%, ZINC OXIDE 1.0%

INGREDIENTS

WATER, CYCLOPENTASILOXANE, TITANIUM DIOXIDE, BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE, BUTYLENE GLYCOL, ETHYLHEXYL METHOXYCINNAMATE, DIMETHICONE, POLYMETHYL METHACRYLATE, LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, MICA, DISTEARDIMONIUM HECTORITE, SODIUM CHLORIDE, MINERAL WATER, CAMELLIA SINENSIS LEAF EXTRACT, BETA-GLUCAN, GLYCERIN, HYDROXYPROPYL BISPALMITAMIDE MEA, POLYGLUTAMIC ACID, LAVANDULA STOECHAS EXTRACT, BORON NITRIDE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, SORBITAN ISOSTEARATE, ZINC OXIDE, POLYSILICONE-11, ALUMINUM HYDROXIDE, ACRYLATES/ETHYLHEXYL ACRYLATE/DIMETHICONE METHACRYLATE COPOLYMER, STEARIC ACID, CAPRYLYL LYCOL, TRIETHOXYCAPRYLYLSILANE, ETHYLHEXYLGLYCERIN, DISODIUM EDTA,MANNAN, IRON OXIDES (CI77491, CI77492, CI77499), FRAGRANCE

PRINCIPAL DISPLAY PANEL - 35mL Bottle Carton - NO. 13

IOPE

IOPE

SMALL&SMOOTH

S.S CONDITIONING
FOUNDATION

IOPE SS

PRINCIPAL DISPLAY PANEL - 35mL Bottle Carton - NO. 21

IOPE

IOPE

SMALL&SMOOTH

S.S CONDITIONING
FOUNDATION

IOPE SS

PRINCIPAL DISPLAY PANEL 35mL Bottle Carton - NO. 23

IOPE

IOPE

SMALL&SMOOTH

S.S CONDITIONING
FOUNDATION

IOPE SS

PRINCIPAL DISPLAY PANEL 35mL Bottle Carton - NO. 31

IOPE

IOPE

SMALL&SMOOTH

S.S CONDITIONING
FOUNDATION

IOPE SS

IOPE SS

Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43419-356
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.05 mL
titanium dioxide 0.03 mL
Zinc Oxide Zinc oxide 0.01 mL

Inactive Ingredients

Ingredient Name Strength
water
MICA
CYCLOMETHICONE 5
BUTYLENE GLYCOL
DIMETHICONE
SODIUM CHLORIDE
GREEN TEA LEAF
GLYCERIN
aluminum hydroxide
STEARIC ACID
ETHYLHEXYLGLYCERIN
EDETATE DISODIUM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43419-356-03 35 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-11-01


IOPE SS

Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43419-357
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.05 mL
titanium dioxide 0.03 mL
Zinc Oxide Zinc oxide 0.01 mL

Inactive Ingredients

Ingredient Name Strength
water
MICA
CYCLOMETHICONE 5
BUTYLENE GLYCOL
DIMETHICONE
SODIUM CHLORIDE
GREEN TEA LEAF
GLYCERIN
aluminum hydroxide
STEARIC ACID
ETHYLHEXYLGLYCERIN
EDETATE DISODIUM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43419-357-04 35 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-11-01


IOPE SS

Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43419-358
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.05 mL
titanium dioxide 0.03 mL
Zinc Oxide Zinc oxide 0.01 mL

Inactive Ingredients

Ingredient Name Strength
water
MICA
CYCLOMETHICONE 5
BUTYLENE GLYCOL
DIMETHICONE
SODIUM CHLORIDE
GREEN TEA LEAF
GLYCERIN
aluminum hydroxide
STEARIC ACID
ETHYLHEXYLGLYCERIN
EDETATE DISODIUM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43419-358-05 35 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-11-01


IOPE SS

Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43419-359
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.05 mL
titanium dioxide 0.03 mL
Zinc Oxide Zinc oxide 0.01 mL

Inactive Ingredients

Ingredient Name Strength
water
MICA
CYCLOMETHICONE 5
BUTYLENE GLYCOL
DIMETHICONE
SODIUM CHLORIDE
GREEN TEA LEAF
GLYCERIN
aluminum hydroxide
STEARIC ACID
ETHYLHEXYLGLYCERIN
EDETATE DISODIUM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43419-359-06 35 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-11-01


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Be sure to consult your doctor before taking any medication!
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