PLACENTA EX SUN BALM SPF50PLUS PA PLUS PLUS PLUS- octinoxate, titanium dioxide, zinc oxide cream

PLACENTA EX SUN BALM by

Drug Labeling and Warnings

PLACENTA EX SUN BALM 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%, Titanium Dioxide 6.1%, Zinc Oxide 4.9%

INACTIVE INGREDIENT

Inactive Ingredients:
Dicaprylyl Carbonate, Silica, Caprylic/Capric Triglyceride, Methicone, Aluminum Hydroxide, Stearic Acid, Mica, Triethoxycaprylylsilane, Ceresin, Dimethicone, Isoamyl p-Methoxycinnamate, Microcrystalline Wax, Polyethylene, Hydroxyapatite, Sorbitan Isostearate, Cetearyl Glucoside, Cetearyl Alcohol, Triethoxycaprylylsilane, Acetylated Sucrose Distearate, Cyclopentasiloxane, C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Methyl Methacrylate Crosspolymer, Ultramarines, Fragrance, Methylparaben, Butylene Glycol, Water, Glycine Soja (Soybean)Phytoplacenta Extract, Iron Oxides, Alcohol, Gentiana Lutea Root Extract, Achillea Millefolium Extract, Artemisia Absinthium Extract, Arnica Montana Flower Extract, Potassium Sorbate, Citrus Aurantium Dulcis (Orange) Fruit Water, 1,2-Hexanediol, Hydrolyzed Collagen

PURPOSE

Purpose: Sunscreen product with multi-functions of brightening and anti-aging care.

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 an appropriate amount to the face using a gentle patting motion.

DOSAGE AND ADMINISTRATION

How to Use: Apply an appropriate amount to the face using a gentle patting motion.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PLACENTA EX SUN BALM  SPF50PLUS PA PLUS PLUS PLUS
octinoxate, titanium dioxide, zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51346-031
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.84 g  in 12 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	0.73 g  in 12 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.59 g  in 12 g

Inactive Ingredients
Ingredient Name	Strength
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
STEARIC ACID (UNII: 4ELV7Z65AP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51346-031-01	12 g in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	03/01/2012

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(51346-031)