BROCCOLI SUN description, usages, side effects, indications, overdosage, supplying and lots more!

BROCCOLI SUN

SKINFOOD CO., LTD.
SKINFOOD CO., LTD.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Drug Facts



FULL PRESCRIBING INFORMATION

Active ingredient

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

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.

Uses

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

OCTINOXATE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:76214-018
Route of Administration CUTANEOUS DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 2.5 mL
OCTISALATE OCTISALATE 2.5 mL
Zinc Oxide Zinc oxide 1.9 mL
titanium dioxide 1.44 mL

Inactive Ingredients

Ingredient Name Strength
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 Code Package Description Marketing Start Date Marketing End Date
1 NDC:76214-018-01 50 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-03-01


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