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

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GOLDKIWI SUN

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

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients: OCTINOXATE 7%, ZINC OXIDE 4.9%, TITANIUM DIOXIDE 4.15%

Inactive ingredients:
Dimethicone, Triethylhexanoin, Silica, Talc, Phenyl Trimethicone, Isoamyl p-Methoxycinnamate, Polyethylene, Ceresin, Sorbitan Isostearate, Microcrystalline Wax, Vinyl Dimethicone/Methicone Silsesquiox ane Crosspolymer, Aluminum Hydroxide, Stearic Acid, Triethoxycaprylylsilane, Fragrance(Parfum), Polyglyceryl-2 Triisostearate, Iron Oxides (CI 77492), Glyceryl Caprylate, Caprylyl Glycol, Iron Oxides (CI 77491), Actinidia Chinensis (Kiwi) Fruit Extract, Argania Spinosa Kernel Oil, Hydroxyapatite, Helianthus Annuus (Sunflower) Seed Oil

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:
At the end of basic cosmetic care, apply in an adequate amount to body parts sensitive to UV radiation such as face, arms and legs, avoiding the eye area

Dosage and administration:
Apply about 15 to 20 minutes before going out.
Reapply as often as possible for a long-term outing or activities.

GOLDKIWI SUN

GOLDKIWI SUN

OCTINOXATE STICK

Product Information

Product Type Human otc drug label Item Code (Source) NDC:76214-039
Route of Administration CUTANEOUS DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 1.47 g
Zinc Oxide Zinc oxide 1.03 g
titanium dioxide 0.87 g

Inactive Ingredients

Ingredient Name Strength
DIMETHICONE
TRIETHYLHEXANOIN
SILICON DIOXIDE
talc
PHENYL TRIMETHICONE
Ceresin
aluminum hydroxide
STEARIC ACID
TRIETHOXYCAPRYLYLSILANE
GLYCERYL CAPRYLATE
CAPRYLYL GLYCOL
KIWI FRUIT
ARGAN OIL
SUNFLOWER OIL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:76214-039-01 21 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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