NDC 51346-063 Placenta Ex Essence

NDC Product Code 51346-063

NDC 51346-063-01

Package Description: 40 mL in 1 CARTON

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Placenta Ex Essence with NDC 51346-063 is a product labeled by Nature Republic Co., Ltd.. The generic name of Placenta Ex Essence is . The product's dosage form is and is administered via form.

Labeler Name: Nature Republic Co., Ltd.

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Nature Republic Co., Ltd.
Labeler Code: 51346
Start Marketing Date: 10-01-2010 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2018 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Placenta Ex Essence Product Label Images

Placenta Ex Essence Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Active Ingredient: Dimethicone 1%

Inactive Ingredient

Inactive Ingredients:Water, Glycerin, Cyclopentasiloxane, Dimethicone/Vinyl Dimethicone Crosspolymer, Butylene Glycol, Caprylyl Methicone, Hydrogenated Polyisobutene, Niacinamide, Beheneth-10, Paraffin, Methyl Gluceth-20, HDI/Trimethylol Hexyllactone Crosspolymer, Silica, 1,2-Hexanediol, Hydrolyzed Collagen, Glycine Soja (Soybean)Phytoplacenta Extract, Sodium Polyacrylate, Phenoxyethanol, Lithium Magnesium Sodium Silicate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Glyceryl Caprylate, Caprylyl Glycol, Fragrance, 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, Yellow 6


Purpose: Brightening and wrinkle improvement.


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


Indications And Usage

How to Use: After using our toner, dispense 1-2 pumps and apply to the entire face.

Dosage And Administration

How to Use: After using our toner, dispense 1-2 pumps and apply to the entire face.

* Please review the disclaimer below.