SENSAI FLUID FINISH LASTING VELVET FV102 description, usages, side effects, indications, overdosage, supplying and lots more!

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SENSAI FLUID FINISH LASTING VELVET FV102

KANEBO COSMETICS INC

SENSAI SPF 15 FLUID FINISH LASTING VELVET


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Direction

Apply liberally and evenly before sun exposure and as needed.

Use helps prevent sunburn.

Apply and reapply as directed to avoid lowering protection.

ACTIVE INGREDIENTS

OCTINOXATE 4.0% Sunscreen

TITANIUM DIOXIDE 4.4% Sunscreen

INGREDIENTS

WATER (AQUA), DIMETHICONE, TITANIUM DIOXIDE, ETHYLHEXYL METHOXYCINNAMATE, DIPROPYLENE GLYCOL, METHYL TRIMETHICONE, ACRYLATES COPOLYMER, HYDROGENATED POLYDECENE, CYCLOMETHICONE, PHENYL TRIMETHICONE, MALTITOL, NYLON-12, SORBITAN ISOSTEARATE, POLYPROPYLSILSESQUIOXANE, SODIUM CHLORIDE, TRIFLUOROPROPYL DIMETHICONOL, ALUMINUM HYDROXIDE, DIMETHICONE COPOLYOL, ISOPROPYL TITANIUM TRIISOSTEARATE, HYDROGENATED LECITHIN, SILICA, HYDRATED SILICA, SQUALANE, LAUROYL LYSINE, SODIUM LAUROYL ASPARTATE, FRAGRANCE (PARFUM), DISTEARYLDIMONIUM CHLORIDE,ZINC CHLORIDE, ALCOHOL, HYDROLYZED SILK, BHT,ISOPROPYL ALCOHOL, HYDROLYZED RICE EXTRACT, OCTYLDODECYL LACTATE, STEARIC ACID, MYRISTIC ACID, TOCOPHEROL, PHENOXYETHANOL, METHYLPARABEN, ETHYLPARABEN, BUTYLPARABEN,
[MAY CONTAIN(+/-):
IRON OXIDES (CI 77491), IRON OXIDES (CI 77492), IRON OXIDES (CI 77499), MICA (CI 77019), TALC, ZINC OXIDE (CI 77947) ]

WARNING

For external use only. Keep out of eyes. Rinse with water to remove.

If a rash appears on the skin, stop use and consult a doctor.

Keep out of reach of children.

PRINCIPAL DISPLAY PANEL - 30mL Ivory Soft Carton

SENSAI

SPF 15

FLUID FINISH
LASTING VELVET

Kanebo
INTERNATIONAL

NET 1.02 FL.OZ. 30mL e

SENSAI FLUID FINISH LASTING VELVET FV102

PRINCIPAL DISPLAY PANEL - 30mL Warm Beige Carton

SENSAI

SPF 15

FLUID FINISH
LASTING VELVET

Kanebo
INTERNATIONAL

NET 1.02 FL.OZ. 30mL e

SENSAI FLUID FINISH LASTING VELVET FV102

PRINCIPAL DISPLAY PANEL - 30mL Soft Beige Carton

SENSAI

SPF 15

FLUID FINISH
LASTING VELVET

Kanebo
INTERNATIONAL

NET 1.02 FL.OZ. 30mL e

SENSAI FLUID FINISH LASTING VELVET FV102

PRINCIPAL DISPLAY PANEL - 30mL Natural Beige Carton

SENSAI

SPF 15

FLUID FINISH
LASTING VELVET

Kanebo
INTERNATIONAL

NET 1.02 FL.OZ. 30mL e

SENSAI FLUID FINISH LASTING VELVET FV102

PRINCIPAL DISPLAY PANEL - 30mL Almond Beige Carton

SENSAI

SPF 15

FLUID FINISH
LASTING VELVET

Kanebo
INTERNATIONAL

NET 1.02 FL.OZ. 30mL e

SENSAI FLUID FINISH LASTING VELVET FV102

PRINCIPAL DISPLAY PANEL - 30mL Amber Beige Carton

SENSAI

SPF 15

FLUID FINISH
LASTING VELVET

Kanebo
INTERNATIONAL

NET 1.02 FL.OZ. 30mL e

SENSAI FLUID FINISH LASTING VELVET FV102

PRINCIPAL DISPLAY PANEL - 30mL Topaz Beige Carton

SENSAI

SPF 15

FLUID FINISH
LASTING VELVET

Kanebo
INTERNATIONAL

NET 1.02 FL.OZ. 30mL e

SENSAI FLUID FINISH LASTING VELVET FV102

PRINCIPAL DISPLAY PANEL - 30mL Golden Dune Carton

SENSAI

SPF 15

FLUID FINISH
LASTING VELVET

Kanebo
INTERNATIONAL

NET 1.02 FL.OZ. 30mL e

SENSAI FLUID FINISH LASTING VELVET FV102

SENSAI FLUID FINISH LASTING VELVET FV102

TITANIUM DIOXIDE and OCTINOXATE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64159-7695
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
titanium dioxide 4.4 g
OCTINOXATE OCTINOXATE 4 g

Inactive Ingredients

Ingredient Name Strength
water
DIMETHICONE
DIPROPYLENE GLYCOL
METHYL TRIMETHICONE
cyclomethicone
PHENYL TRIMETHICONE
MALTITOL
NYLON-12
Sorbitan Isostearate
SODIUM CHLORIDE
aluminum hydroxide
SILICON DIOXIDE
HYDRATED SILICA
SQUALANE
LAUROYL LYSINE
SODIUM LAUROYL ASPARTATE
DISTEARYLDIMONIUM CHLORIDE
ZINC CHLORIDE
ALCOHOL
BUTYLATED HYDROXYTOLUENE
ISOPROPYL ALCOHOL
OCTYLDODECYL LACTATE
STEARIC ACID
MYRISTIC ACID
Tocopherol
PHENOXYETHANOL
METHYLPARABEN
ETHYLPARABEN
BUTYLPARABEN
ferric oxide red
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
MICA
talc
Zinc Oxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64159-7695-1 30 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-08-01


SENSAI FLUID FINISH LASTING VELVET FV103

TITANIUM DIOXIDE and OCTINOXATE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64159-7696
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
titanium dioxide 4.4 g
OCTINOXATE OCTINOXATE 4 g

Inactive Ingredients

Ingredient Name Strength
water
DIMETHICONE
DIPROPYLENE GLYCOL
METHYL TRIMETHICONE
cyclomethicone
PHENYL TRIMETHICONE
MALTITOL
NYLON-12
Sorbitan Isostearate
SODIUM CHLORIDE
aluminum hydroxide
SILICON DIOXIDE
HYDRATED SILICA
SQUALANE
LAUROYL LYSINE
SODIUM LAUROYL ASPARTATE
DISTEARYLDIMONIUM CHLORIDE
ZINC CHLORIDE
ALCOHOL
BUTYLATED HYDROXYTOLUENE
ISOPROPYL ALCOHOL
OCTYLDODECYL LACTATE
STEARIC ACID
MYRISTIC ACID
Tocopherol
PHENOXYETHANOL
METHYLPARABEN
ETHYLPARABEN
BUTYLPARABEN
ferric oxide red
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
MICA
talc
Zinc Oxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64159-7696-1 30 in 1 BOTTLE, GLASS
2 NDC:64159-7696-2 12 in 1 BOTTLE, GLASS
3 NDC:64159-7696-3 2 in 1 BOTTLE, PLASTIC
4 NDC:64159-7696-4 0.7 in 1 POUCH

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-08-01


SENSAI FLUID FINISH LASTING VELVET FV202

TITANIUM DIOXIDE and OCTINOXATE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64159-7697
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
titanium dioxide 4.4 g
OCTINOXATE OCTINOXATE 4 g

Inactive Ingredients

Ingredient Name Strength
water
DIMETHICONE
DIPROPYLENE GLYCOL
METHYL TRIMETHICONE
cyclomethicone
PHENYL TRIMETHICONE
MALTITOL
NYLON-12
Sorbitan Isostearate
SODIUM CHLORIDE
aluminum hydroxide
SILICON DIOXIDE
HYDRATED SILICA
SQUALANE
LAUROYL LYSINE
SODIUM LAUROYL ASPARTATE
DISTEARYLDIMONIUM CHLORIDE
ZINC CHLORIDE
ALCOHOL
BUTYLATED HYDROXYTOLUENE
ISOPROPYL ALCOHOL
OCTYLDODECYL LACTATE
STEARIC ACID
MYRISTIC ACID
Tocopherol
PHENOXYETHANOL
METHYLPARABEN
ETHYLPARABEN
BUTYLPARABEN
ferric oxide red
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
MICA
talc
Zinc Oxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64159-7697-1 30 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-08-01


SENSAI FLUID FINISH LASTING VELVET FV203

TITANIUM DIOXIDE and OCTINOXATE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64159-7698
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
titanium dioxide 4.4 g
OCTINOXATE OCTINOXATE 4 g

Inactive Ingredients

Ingredient Name Strength
water
DIMETHICONE
DIPROPYLENE GLYCOL
METHYL TRIMETHICONE
cyclomethicone
PHENYL TRIMETHICONE
MALTITOL
NYLON-12
Sorbitan Isostearate
SODIUM CHLORIDE
aluminum hydroxide
SILICON DIOXIDE
HYDRATED SILICA
SQUALANE
LAUROYL LYSINE
SODIUM LAUROYL ASPARTATE
DISTEARYLDIMONIUM CHLORIDE
ZINC CHLORIDE
ALCOHOL
BUTYLATED HYDROXYTOLUENE
ISOPROPYL ALCOHOL
OCTYLDODECYL LACTATE
STEARIC ACID
MYRISTIC ACID
Tocopherol
PHENOXYETHANOL
METHYLPARABEN
ETHYLPARABEN
BUTYLPARABEN
ferric oxide red
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
MICA
talc
Zinc Oxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64159-7698-1 30 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-08-01


SENSAI FLUID FINISH LASTING VELVET FV204

TITANIUM DIOXIDE and OCTINOXATE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64159-7699
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
titanium dioxide 4.4 g
OCTINOXATE OCTINOXATE 4 g

Inactive Ingredients

Ingredient Name Strength
water
DIMETHICONE
DIPROPYLENE GLYCOL
METHYL TRIMETHICONE
cyclomethicone
PHENYL TRIMETHICONE
MALTITOL
NYLON-12
Sorbitan Isostearate
SODIUM CHLORIDE
aluminum hydroxide
SILICON DIOXIDE
HYDRATED SILICA
SQUALANE
LAUROYL LYSINE
SODIUM LAUROYL ASPARTATE
DISTEARYLDIMONIUM CHLORIDE
ZINC CHLORIDE
ALCOHOL
BUTYLATED HYDROXYTOLUENE
ISOPROPYL ALCOHOL
OCTYLDODECYL LACTATE
STEARIC ACID
MYRISTIC ACID
Tocopherol
PHENOXYETHANOL
METHYLPARABEN
ETHYLPARABEN
BUTYLPARABEN
ferric oxide red
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
MICA
talc
Zinc Oxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64159-7699-1 30 in 1 BOTTLE, GLASS
2 NDC:64159-7699-2 12 in 1 BOTTLE, GLASS
3 NDC:64159-7699-3 2 in 1 BOTTLE, PLASTIC
4 NDC:64159-7699-4 0.7 in 1 POUCH

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-08-01


SENSAI FLUID FINISH LASTING VELVET FV204.5

TITANIUM DIOXIDE and OCTINOXATE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64159-7700
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
titanium dioxide 4.4 g
OCTINOXATE OCTINOXATE 4 g

Inactive Ingredients

Ingredient Name Strength
water
DIMETHICONE
DIPROPYLENE GLYCOL
METHYL TRIMETHICONE
cyclomethicone
PHENYL TRIMETHICONE
MALTITOL
NYLON-12
Sorbitan Isostearate
SODIUM CHLORIDE
aluminum hydroxide
SILICON DIOXIDE
HYDRATED SILICA
SQUALANE
LAUROYL LYSINE
SODIUM LAUROYL ASPARTATE
DISTEARYLDIMONIUM CHLORIDE
ZINC CHLORIDE
ALCOHOL
BUTYLATED HYDROXYTOLUENE
ISOPROPYL ALCOHOL
OCTYLDODECYL LACTATE
STEARIC ACID
MYRISTIC ACID
Tocopherol
PHENOXYETHANOL
METHYLPARABEN
ETHYLPARABEN
BUTYLPARABEN
ferric oxide red
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
MICA
talc
Zinc Oxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64159-7700-1 30 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-08-01


SENSAI FLUID FINISH LASTING VELVET FV205

TITANIUM DIOXIDE and OCTINOXATE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64159-6010
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
titanium dioxide 4.4 g
OCTINOXATE OCTINOXATE 4 g

Inactive Ingredients

Ingredient Name Strength
water
DIMETHICONE
DIPROPYLENE GLYCOL
METHYL TRIMETHICONE
cyclomethicone
PHENYL TRIMETHICONE
MALTITOL
NYLON-12
Sorbitan Isostearate
SODIUM CHLORIDE
aluminum hydroxide
SILICON DIOXIDE
HYDRATED SILICA
SQUALANE
LAUROYL LYSINE
SODIUM LAUROYL ASPARTATE
DISTEARYLDIMONIUM CHLORIDE
ZINC CHLORIDE
ALCOHOL
BUTYLATED HYDROXYTOLUENE
ISOPROPYL ALCOHOL
OCTYLDODECYL LACTATE
STEARIC ACID
MYRISTIC ACID
Tocopherol
PHENOXYETHANOL
METHYLPARABEN
ETHYLPARABEN
BUTYLPARABEN
ferric oxide red
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
MICA
talc
Zinc Oxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64159-6010-1 30 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-08-01


SENSAI FLUID FINISH LASTING VELVET FV206

TITANIUM DIOXIDE and OCTINOXATE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64159-6011
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
titanium dioxide 4.4 g
OCTINOXATE OCTINOXATE 4 g

Inactive Ingredients

Ingredient Name Strength
water
DIMETHICONE
DIPROPYLENE GLYCOL
METHYL TRIMETHICONE
cyclomethicone
PHENYL TRIMETHICONE
MALTITOL
NYLON-12
Sorbitan Isostearate
SODIUM CHLORIDE
aluminum hydroxide
SILICON DIOXIDE
HYDRATED SILICA
SQUALANE
LAUROYL LYSINE
SODIUM LAUROYL ASPARTATE
DISTEARYLDIMONIUM CHLORIDE
ZINC CHLORIDE
ALCOHOL
BUTYLATED HYDROXYTOLUENE
ISOPROPYL ALCOHOL
OCTYLDODECYL LACTATE
STEARIC ACID
MYRISTIC ACID
Tocopherol
PHENOXYETHANOL
METHYLPARABEN
ETHYLPARABEN
BUTYLPARABEN
ferric oxide red
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
MICA
talc
Zinc Oxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64159-6011-1 30 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-08-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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