SENSAI SILKY BRONZE SUN PROTECTIVE EMULSION FOR BODY SPF20 description, usages, side effects, indications, overdosage, supplying and lots more!

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SENSAI SILKY BRONZE SUN PROTECTIVE EMULSION FOR BODY SPF20

KANEBO COSMETICS INC.

SENSAI SILKY BRONZE SPF 20


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS

Purpose

AVOBENZONE 1.2% Sunscreen
OCTINOXATE 4.8% Sunscreen

INGREDIENTS

WATER (AQUA), CYCLOMETHICONE, GLYCERIN, ETHYLHEXYL METHOXYCINNAMATE, DIPROPYLENE GLYCOL, TRIETHYLHEXANOIN, BUTYL METHOXYDIBENZOYLMETHANE, BUTYLENE GLYCOL, CETYL ALCOHOL, GLYCERYL STEARATE, DIMETHICONE, STEARIC ACID, CARBOMER, PALMITIC ACID, OLEYL ALCOHOL, PEG-60 HYDROGENATED CASTOR OIL, XANTHAN GUM, POTASSIUM HYDROXIDE, CETYL PALMITATE, DIPOTASSIUM GLYCYRRHIZATE, METHYLSERINE, NIACINAMIDE, PRUNUS ARMENIACA (APRICOT) KERNEL OIL, FRAGRANCE (PARFUM), ALCOHOL, PRUNUS ARMENIACA (APRICOT) JUICE, MYRISTIC ACID, DISODIUM EDTA, DIMETHOXY DI-p-CRESOL, HYDROLYZED SILK, PYRACANTHA FORTUNEANA FRUIT EXTRACT, PRUNUS ARMENIACA (APRICOT) KERNEL EXTRACT, PRUNUS PERSICA (PEACH) KERNEL EXTRACT, BHT, PHENOXYETHANOL, METHYLPARABEN, ETHYLPARABEN, PROPYLPARABEN, BUTYLPARABEN, BUTYLPHENYL METHYLPROPIONAL, GERANIOL, HEXYL CINNAMAL, LINALOOL

Direction

Apply liberally and evenly before sun exposure and as needed.

Use helps prevent sunburn.

Apply and reapply as directed to avoid lowering protection.

Warning

Stop use and ask a doctor if

  • skin rash occurs.

Keep out of reach of children.

WARNING: Keep out of the eyes. Discontinue use if irritation appears.

DIST.: Kanebo Cosmetics USA, Inc.
330 Madison Avenue, New York, NY 10017

PRINCIPAL DISPLAY PANEL - 150 mL Tube Carton

SENSAI

SILKY BRONZE

SPF 20

SUN PROTECTIVE EMULSION
FOR BODY

ÉMULSION SOLAIRE
PROTECTRICE CORPS

Kanebo
INTERNATIONAL

NET WT. 5.1 OZ. 150mL e

SENSAI SILKY BRONZE SUN PROTECTIVE EMULSION FOR BODY SPF20

SENSAI SILKY BRONZE SUN PROTECTIVE EMULSION FOR BODY SPF20

AVOBENZONE and OCTINOXATE EMULSION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64159-6376
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOBENZONE AVOBENZONE 1.2 g
OCTINOXATE OCTINOXATE 4.8 g

Inactive Ingredients

Ingredient Name Strength
water
cyclomethicone
GLYCERIN
DIPROPYLENE GLYCOL
BUTYLENE GLYCOL
CETYL ALCOHOL
GLYCERYL MONOSTEARATE
DIMETHICONE
STEARIC ACID
METHYLPARABEN
PALMITIC ACID
OLEYL ALCOHOL
POLYOXYL 60 HYDROGENATED CASTOR OIL
XANTHAN GUM
PHENOXYETHANOL
POTASSIUM HYDROXIDE
cetyl palmitate
GLYCYRRHIZINATE DIPOTASSIUM
NIACINAMIDE
APRICOT
ALCOHOL
MYRISTIC ACID
EDETATE DISODIUM
BUTYLATED HYDROXYTOLUENE
PEACH
ETHYLPARABEN
BUTYLPARABEN
PROPYLPARABEN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64159-6376-1 150 in 1 TUBE
2 NDC:64159-6376-2 10 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2007-02-01


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