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 7.5%, ZINC OXIDE 4.90%, TITANIUM DIOXIDE 2.90%

Inactive ingredients:
Water, Cyclopentasiloxane, Ethylhexyl Salicylate, Glycerin, PEG-10 Dimethicone, Dimethicone, Dipropylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Magnesium Sulfate, Disteardimonium Hectorite, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Isoamyl p-Methoxycinnamate, Dimethicone/Vinyl Dimethicone Crosspolymer, Aluminum Hydroxide, Stearic Acid, Methyl Methacrylate Crosspolymer, Methylparaben, Phenoxyethanol, Fragrance(Parfum), Actinidia Chinensis (Kiwi) Fruit Extract, Propylparaben, Caffeine, Sea Water, Polydecene, Squalane, Viscum Album (Mistletoe) Extract, Palmitoyl Tripeptide-5

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 CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:76214-013
Route of Administration CUTANEOUS DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 3.75 g
Zinc Oxide Zinc oxide 2.45 g
titanium dioxide 1.45 g

Inactive Ingredients

Ingredient Name Strength
water
CYCLOMETHICONE 5
GLYCERIN
DIMETHICONE
aluminum hydroxide
STEARIC ACID
METHYLPARABEN
PHENOXYETHANOL
KIWI FRUIT
PROPYLPARABEN
CAFFEINE
SQUALANE
PALMITOYL TRIPEPTIDE-5

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:76214-013-01 50 in 1 CARTON

Marketing Information

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


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