GOLDKIWI SUN SPF 50 PLUS PA PLUS PLUS PLUS- octinoxate stick

GOLDKIWI SUN by

Drug Labeling and Warnings

GOLDKIWI SUN by is a Otc medication manufactured, distributed, or labeled by SKINFOOD CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

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

INACTIVE INGREDIENT

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

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:
Keep out of reach of children.

INDICATIONS & USAGE

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 & ADMINISTRATION

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOLDKIWI SUN  SPF 50 PLUS PA PLUS PLUS PLUS
octinoxate stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76214-039
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.47 g  in 21 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC OXIDE	1.03 g  in 21 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM - UNII:D1JT611TNE)	TITANIUM DIOXIDE	0.87 g  in 21 g

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE (UNII: 92RU3N3Y1O)
TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TALC (UNII: 7SEV7J4R1U)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
CERESIN (UNII: Q1LS2UJO3A)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
STEARIC ACID (UNII: 4ELV7Z65AP)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
KIWI FRUIT (UNII: 71ES77LGJC)
ARGAN OIL (UNII: 4V59G5UW9X)
SUNFLOWER OIL (UNII: 3W1JG795YI)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	03/01/2011

Labeler - SKINFOOD CO., LTD. (690324173)

Registrant - SKINFOOD CO., LTD. (690324173)

Establishment
Name	Address	ID/FEI	Business Operations
SKINFOOD CO., LTD.		690324173	manufacture