SENSAI SILKY BRONZE SUN PROTECTIVE EMULSION FOR BODY SPF20

Dosage form: emulsion
Ingredients: AVOBENZONE 1.2g in 100mL, OCTINOXATE 4.8g in 100mL
Labeler: KANEBO COSMETICS INC.
NDC Code: 64159-6376

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.

SENSAI
SILKY BRONZE
SPF 20

ACTIVE INGREDIENTS

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 
avobenzone and octinoxate emulsion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64159-6376
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (AVOBENZONE) AVOBENZONE1.2 g  in 100 mL
OCTINOXATE (OCTINOXATE) OCTINOXATE4.8 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage Description
1NDC:64159-6376-1150 mL in 1 TUBE
2NDC:64159-6376-210 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35202/01/2007
Labeler - KANEBO COSMETICS INC. (691041271)

Revised: 12/2011
 
KANEBO COSMETICS INC.

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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