UV LOCK FLOWER DAILY POWERFUL SUN SPF50PLUS PA PLUS PLUS PLUS- octinoxate, octisalate, zinc oxide, titanium dioxide cream

UV LOCK FLOWER DAILY POWERFUL SUN by

Drug Labeling and Warnings

UV LOCK FLOWER DAILY POWERFUL 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%, ETHYLHEXYL SALICYLATE 5%, ZINC OXIDE 4.8%, TITANIUM DIOXIDE 2.5%

INACTIVE INGREDIENT

Inactive Ingredients:
WATER, CYCLOPENTASILOXANE, GLYCERIN, DIPROPYLENE GLYCOL, PEG-10 DIMETHICONE, DIMETHICONE, TALC, DISTEARDIMONIUM HECTORITE, ISODECYL NEOPENTANOATE, OCTYLDODECYL NEOPENTANOATE, MAGNESIUM SULFATE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, PHENOXYETHANOL, METHYL METHACRYLATE CROSSPOLYMER, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, METHICONE, FRAGRANCE, METHYLPARABEN, POLYGLYCERYL-6 POLYRICINOLEATE, PROPYLPARABEN, SEA WATER, TRIHYDROXYSTEARIN,
IRON OXIDES, ALOE BARBADENSIS LEAF JUICE, CENTELLA ASIATICA EXTRACT, HAMAMELIS VIRGINIANA (WITCH HAZEL) BARK/LEAF/TWIG EXTRACT, HEDERA HELIX (IVY) EXTRACT, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, MACADAMIA TERNIFOLIA SEED OIL, BUTYLPARABEN

PURPOSE

Purpose: Powerful sunscreen to protect your skin from the scorching summer sun.

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: Apply evenly before sun exposure.

DOSAGE & ADMINISTRATION

How to Use: Apply evenly before sun exposure.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UV LOCK FLOWER DAILY POWERFUL SUN  SPF50PLUS PA PLUS PLUS PLUS
octinoxate, octisalate, zinc oxide, titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51346-038
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	3.75 g  in 50 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	2.50 g  in 50 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	2.40 g  in 50 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1.25 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
GLYCERIN (UNII: PDC6A3C0OX)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
DIMETHICONE (UNII: 92RU3N3Y1O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51346-038-01	50 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(51346-038)