BROCCOLI SUN SPF42 PA PLUS PLUS PLUS

Dosage form: cream
Ingredients: OCTINOXATE 2.5mL in 50mL, OCTISALATE 2.5mL in 50mL, ZINC OXIDE 1.9mL in 50mL, TITANIUM DIOXIDE 1.44mL in 50mL
Labeler: SKINFOOD CO., LTD.
NDC Code: 76214-018

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.

Drug Facts

Active ingredients: OCTINOXATE 5%, OCTISALATE 5%, ZINC OXIDE 3.8%, TITANIUM DIOXIDE 2.87%

Inactive ingredients:
WATER, CYCLOPENTASILOXANE, C12-15 ALKYL BENZOATE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, DIETHYLHEXYL CARBONATE, ISOAMYL p-METHOXYCINNAMATE, CETYL CAPRYLATE, DIMETHICONE, CYCLOHEXASILOXANE, CETYL PEG/PPG-10/1 DIMETHICONE, STEARALKONIUM HECTORITE, POLYGLYCERYL-6 POLYHYDROXYSTEARATE,
PEG-30 DIPOLYHYDROXYSTEARATE, SODIUM CHLORIDE, PEG-10 DIMETHICONE, OZOKERITE, PROPYLENE CARBONATE, POLYGLYCERYL-4 ISOSTEARATE, SORBITAN SESQUIOLEATE, ALCOHOL DENAT., HEXYL LAURATE, SORBITAN OLIVATE, TRIMETHOXYCAPRYLYLSILANE, DIMETHICONE, ALOE BARBADENSIS LEAF EXTRACT, BRASSICA OLERACEA ITALICA (BROCCOLI) EXTRACT, BUTYLENE GLYCOL, CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT, PORTULACA OLERACEA EXTRACT, PROPYLENE GLYCOL, DISODIUM EDTA, METHYLPARABEN, BUTYLPARABEN, FRAGRANCE

Purpose: Protects skin from UV rays.

Warnings:
For external use only. Avoid contact with eyes.
Discontinue use if signs of irritation appear.

Keep out of reach of children:
Keep out of reach of children.

Indication and usage: Use at the end of your daily skincare regimen. Apply liberally onto face and body before sun exposure avoiding the eye area.

Dosage and administration:
For best results, apply at least 15 to 20 minutes before sun exposure.
Reapply frequently while out in the sun.

BROCCOLI SUN  SPF42 PA PLUS PLUS PLUS
octinoxate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76214-018
Route of AdministrationCUTANEOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (OCTINOXATE) OCTINOXATE2.5 mL  in 50 mL
OCTISALATE (OCTISALATE) OCTISALATE2.5 mL  in 50 mL
ZINC OXIDE (ZINC CATION) ZINC OXIDE1.9 mL  in 50 mL
TITANIUM DIOXIDE (TITANIUM) TITANIUM DIOXIDE1.44 mL  in 50 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CYCLOMETHICONE 5 
ALKYL (C12-15) BENZOATE 
BEMOTRIZINOL 
DIETHYLHEXYL CARBONATE 
CETYL OCTANOATE 
DIMETHICONE 
CYCLOMETHICONE 6 
PEG-30 DIPOLYHYDROXYSTEARATE 
SODIUM CHLORIDE 
PROPYLENE CARBONATE 
POLYGLYCERYL-4 ISOSTEARATE 
SORBITAN SESQUIOLEATE 
HEXYL LAURATE 
SORBITAN OLIVATE 
TRIMETHOXYCAPRYLYLSILANE 
METHYLPARABEN 
ALOE VERA LEAF 
BROCCOLI 
BUTYLENE GLYCOL 
BUTYLPARABEN 
MATRICARIA RECUTITA 
PURSLANE 
PROPYLENE GLYCOL 
EDETATE DISODIUM 
Packaging
#Item CodePackage Description
1NDC:76214-018-0150 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35203/01/2011
Labeler - SKINFOOD CO., LTD. (690324173)
Registrant - SKINFOOD CO., LTD. (690324173)
Establishment
NameAddressID/FEIOperations
SKINFOOD CO., LTD.690324173manufacture

Revised: 09/2011
 
SKINFOOD CO., LTD.

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.

Hide
(web5)