UV LOCK ULTRA MILK SUN BIG SIZE SPF50PLUS PA PLUS PLUS PLUS- octinoxate, zinc oxide, octisalate, titanium dioxide cream

UV LOCK ULTRA MILK SUN by

Drug Labeling and Warnings

UV LOCK ULTRA MILK SUN by is a Otc medication manufactured, distributed, or labeled by NATURE REPUBLIC CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients: ETHYLHEXYL METHOXYCINNAMATE 7.5%, ZINC OXIDE 6.5%, ETHYLHEXYL SALICYLATE 5%, TITANIUM DIOXIDE 2.5%

INACTIVE INGREDIENT

Inactive Ingredients:
WATER, CYCLOPENTASILOXANE, ALCOHOL,BUTYLENE GLYCOL, DIPROPYLENE GLYCOL, ISODECYL NEOPENTANOATE, METHYL METHACRYLATE CROSSPOLYMER, PEG-10 DIMETHICONE, MAGNESIUM SULFATE, PHENOXYETHANOL, CALCIUM ALUMINUM BOROSILICATE, FRAGRANCE, METHICONE, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, SILICA, CAPRYLYL GLYCOL, GLYCERYL CAPRYLATE, POLYGLYCERYL-6 POLYRICINOLEATE, OPUNTIA FICUS-INDICA EXTRACT, PORTULACA OLERACEA EXTRACT, ARNICA MONTANA FLOWER EXTRACT, CENTAUREA CYANUS FLOWER EXTRACT, DIANTHUS CARYOPHYLLUS FLOWER EXTRACT, FREESIA REFRACTA EXTRACT, IRIS VERSICOLOR EXTRACT, JASMINUM OFFICINALE (JASMINE) FLOWER/LEAF EXTRACT, ZANTEDESCHIA AETHIOPICA FLOWER/STEM EXTRACT, CELLULOSE GUM, MICROCRYSTALLINE CELLULOSE

PURPOSE

Purpose: Strong milk sun block with daily skincare effects.

WARNINGS

Cautions:
For external use only.
Avoid contact with eyes and mouth.
Discontinue use if signs of irritation or rash appear.
Keep out of reach of children.
Replace the cap after use.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

How to Use: Shake 3-5 times before use. Evenly apply an appropriate amount to skin that is exposed to UV rays.

DOSAGE AND ADMINISTRATION

How to Use: Shake 3-5 times before use. Evenly apply an appropriate amount to skin that is exposed to UV rays.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UV LOCK ULTRA MILK SUN  BIG SIZE SPF50PLUS PA PLUS PLUS PLUS
octinoxate, zinc oxide, octisalate, titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51346-043
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	5.25 g  in 70 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	4.55 g  in 70 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	3.50 g  in 70 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1.75 g  in 70 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
ALCOHOL (UNII: 3K9958V90M)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
DIPROPYLENE GLYCOL (UNII: E107L85C40)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51346-043-01	70 mL in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	01/02/2012

Labeler - NATURE REPUBLIC CO., LTD. (631172020)

Registrant - NATURE REPUBLIC CO., LTD. (631172020)

Establishment
Name	Address	ID/FEI	Business Operations
NATURE REPUBLIC CO., LTD.		631172020	manufacture(51346-043)