UV LOCK ULTRA PACT SUN SPF50PLUS PA PLUS PLUS PLUS- titanium dioxide, octinoxate, zinc oxide powder

UV LOCK ULTRA PACT SUN by

Drug Labeling and Warnings

UV LOCK ULTRA PACT 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: TITANIUM DIOXIDE 7.7%, ETHYLHEXYL METHOXYCINNAMATE 3%, ZINC OXIDE 2.9%

INACTIVE INGREDIENT

Inactive Ingredients:
MICA, TALC, SILICA, DIMETHICONE, NYLON-12, BISMUTH OXYCHLORIDE, MAGNESIUM STEARATE, TRIETHOXYCAPRYLYLSILANE, PHENYL METHICONE, CAPRYLIC/CAPRIC TRIGLYCERIDE, LAUROYL LYSINE, SQUALANE, DIPHENYL DIMETHICONE/VINYL DIPHENYL DIMETHICONE/SILSESQUIOXANE CROSSPOLYMER, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, DIISOSTEARYL MALATE, LANOLIN WAX, IRON OXIDES, ALUMINUM MYRISTATE, FRAGRANCE, METHICONE, METHYLPARABEN, ALLANTOIN, TOCOPHERYL ACETATE, 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, C9-15 FLUOROALCOHOL PHOSPHATE, PROPYLPARABEN, WATER, BUTYLENE GLYCOL

PURPOSE

Purpose: Pact type sun block for UV ray protection, especially effective for touchup.

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

DOSAGE AND ADMINISTRATION

How to Use:
Turn the cap a little to open, and hold the upper cover with the puff.
Dispense an appropriate amount on the puff, and apply it to the entire face with a tapping motion.

INDICATIONS AND USAGE

How to Use:
Turn the cap a little to open, and hold the upper cover with the puff.
Dispense an appropriate amount on the puff, and apply it to the entire face with a tapping motion.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UV LOCK ULTRA PACT SUN  SPF50PLUS PA PLUS PLUS PLUS
titanium dioxide, octinoxate, zinc oxide powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51346-041
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	0.62 g  in 8 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.24 g  in 8 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.23 g  in 8 g

Inactive Ingredients
Ingredient Name	Strength
MICA (UNII: V8A1AW0880)
TALC (UNII: 7SEV7J4R1U)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
DIMETHICONE (UNII: 92RU3N3Y1O)
BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51346-041-01	8 g 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(51346-041)