UV LOCK FLOWER KIDS AND JUNIOR SUN SPF35 PA PLUS PLUS- octinoxate, titanium dioxide cream

UV LOCK FLOWER KIDS AND JUNIOR SUN by

Drug Labeling and Warnings

UV LOCK FLOWER KIDS AND JUNIOR 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%, Titanium Dioxide 2.1%

INACTIVE INGREDIENT

Inactive Ingredients:
Water, Cyclopentasiloxane, Cyclohexasiloxane, Dipropylene Glycol, Butylene Glycol, Dicaprylyl Carbonate, Silica, Dimethicone, Octocrylene, Glycol Stearate, Triceteareth-4 Phosphate, PEG-2 Stearate, Ethylhexyl Palmitate, Cetearyl Alcohol, Butyl Methoxydibenzoylmethane, Glyceryl Stearate, PEG-100 Stearate, Triethanolamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Methylparaben, Phenoxyethanol, Fragrance, Propylparaben, Xanthan Gum, Potassium Cetyl Phosphate, Disodium EDTA, Aloe Barbadensis Leaf Juice, Potassium Sorbate, Sodium Benzoate, Portulaca Oleracea Extract, Helianthus Annuus (Sunflower) Seed Oil, Carapa Guaianensis Seed Oil

PURPOSE

Purpose: Mild kids sun block cream for sensitive skin.

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 the cream to the face and the entire body that will be exposed to UV rays, excluding the skin around the eyes.

DOSAGE AND ADMINISTRATION

How to Use: Apply the cream to the face and the entire body that will be exposed to UV rays, excluding the skin around the eyes.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UV LOCK FLOWER KIDS AND JUNIOR SUN  SPF35 PA PLUS PLUS
octinoxate, titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51346-039
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
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1.05 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51346-039-01	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(51346-039)