PLACENTA EX DAY SPF30 PA PLUS PLUS- octinoxate cream

PLACENTA EX DAY by

Drug Labeling and Warnings

PLACENTA EX DAY 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 Ingredient: Ethylhexyl Methoxycinnamate 7.5%

INACTIVE INGREDIENT

Inactive Ingredients:
Water, Glycerin, Dimethicone, Butyrospermum Parkii (Shea) Butter, Macadamia Integrifolia Seed Oil, 4-Methylbenzylidene Camphor, Diisostearyl Malate, Cetyl Alcohol, Mineral Oil, Arbutin, Butylene Glycol, Isoamyl p-Methoxycinnamate, Octocrylene, Cyclopentasiloxane, Dimethicone/Vinyl Dimethicone Crosspolymer, Butyl Methoxydibenzoylmethane, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Glyceryl Stearate, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Fragrance, Butylene Glycol, Glycine Soja (Soybean) Phytoplacenta Extract,
Phenoxyethanol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Glyceryl Caprylate, Caprylyl Glycol, Xanthan Gum, Adenosine, Disodium EDTA, 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, Yellow 6

PURPOSE

Purpose: Brightening, wrinkle improvement as a multi-functional skincare product.

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: As the last step of skincare in the morning, apply an appropriate amount to the entire face.

DOSAGE AND ADMINISTRATION

How to Use: As the last step of skincare in the morning, apply an appropriate amount to the entire face.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PLACENTA EX DAY  SPF30 PA PLUS PLUS
octinoxate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51346-029
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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHICONE (UNII: 92RU3N3Y1O)
SHEA BUTTER (UNII: K49155WL9Y)
CETYL ALCOHOL (UNII: 936JST6JCN)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51346-029-01	50 mL in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	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(51346-029)