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 TWIN CAKE


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 6.0%, ZINC OXIDE 3.0%

INGREDIENTS

TALC, MICA, TITANIUM DIOXIDE, ETHYLHEXYL METHOXYCINNAMATE, NYLON-12, ZINC OXIDE, SILICA, BORON NITRIDE, CAMELLIA SINENSIS LEAF EXTRACT, LAVANDULA STOECHAS EXTRACT, BETA-GLUCAN, GLYCERIN, POLYGLUTAMIC ACID, PHENYL TRIMETHICONE, TRIETHOXYCAPRYLYLSILANE, DIMETHICONE, LAURYL POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, SQUALANE, METHICONELAUROYL LYSINE, DIISOSTEARYL MALATE, GLYCERYL CAPRYLATE, ETHYLHEXYLGLYCERIN, MAGNESIUM STEARATE, ALUMINUM STEARATE,MINERAL WATER, WATER, ZINC STEARATE, HYDROXYPROPYL BISPALMITAMIDE MEA, IRON OXIDES (CI77492, CI77491, CI77499), ULTRAMARINES, FRAGRANCE

PRINCIPAL DISPLAY PANEL -14g Container Carton - NO. 13

IOPE

IOPE

SMALL&SMOOTH

S.S CONDITIONING
TWIN CAKE

IOPE SS

PRINCIPAL DISPLAY PANEL -14g Container Carton - NO. 21

IOPE

IOPE

SMALL&SMOOTH

S.S CONDITIONING
TWIN CAKE

IOPE SS

PRINCIPAL DISPLAY PANEL - 14g Container Carton - NO. 23

IOPE

IOPE

SMALL&SMOOTH

S.S CONDITIONING
TWIN CAKE

IOPE SS

PRINCIPAL DISPLAY PANEL - 14g Container Carton - NO. 31

IOPE

IOPE

SMALL&SMOOTH

S.S CONDITIONING
TWIN CAKE

IOPE SS

IOPE SS

OCTINOXATE and ZINC OXIDE POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43419-360
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.06 g
Zinc Oxide Zinc oxide 0.03 g

Inactive Ingredients

Ingredient Name Strength
talc
MICA
titanium dioxide
SILICON DIOXIDE
GREEN TEA LEAF
GLYCERIN
PHENYL TRIMETHICONE
DIMETHICONE
SQUALANE
GLYCERYL CAPRYLATE
ETHYLHEXYLGLYCERIN
MAGNESIUM STEARATE
aluminum stearate
water
ZINC STEARATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43419-360-07 14 in 1 CONTAINER

Marketing Information

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


IOPE SS

OCTINOXATE and ZINC OXIDE POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43419-361
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.06 g
Zinc Oxide Zinc oxide 0.03 g

Inactive Ingredients

Ingredient Name Strength
talc
MICA
titanium dioxide
SILICON DIOXIDE
GREEN TEA LEAF
GLYCERIN
PHENYL TRIMETHICONE
DIMETHICONE
SQUALANE
GLYCERYL CAPRYLATE
ETHYLHEXYLGLYCERIN
MAGNESIUM STEARATE
aluminum stearate
water
ZINC STEARATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43419-361-08 14 in 1 CONTAINER

Marketing Information

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


IOPE SS

OCTINOXATE and ZINC OXIDE POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43419-362
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.06 g
Zinc Oxide Zinc oxide 0.03 g

Inactive Ingredients

Ingredient Name Strength
talc
MICA
titanium dioxide
SILICON DIOXIDE
GREEN TEA LEAF
GLYCERIN
PHENYL TRIMETHICONE
DIMETHICONE
SQUALANE
GLYCERYL CAPRYLATE
ETHYLHEXYLGLYCERIN
MAGNESIUM STEARATE
aluminum stearate
water
ZINC STEARATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43419-362-09 14 in 1 CONTAINER

Marketing Information

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


IOPE SS

OCTINOXATE and ZINC OXIDE POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43419-363
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.06 g
Zinc Oxide Zinc oxide 0.03 g

Inactive Ingredients

Ingredient Name Strength
talc
MICA
titanium dioxide
SILICON DIOXIDE
GREEN TEA LEAF
GLYCERIN
PHENYL TRIMETHICONE
DIMETHICONE
SQUALANE
GLYCERYL CAPRYLATE
ETHYLHEXYLGLYCERIN
MAGNESIUM STEARATE
aluminum stearate
water
ZINC STEARATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43419-363-10 14 in 1 CONTAINER

Marketing Information

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


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