NDC 51346-064 Placenta Ex Emulsion

NDC Product Code 51346-064

NDC 51346-064-01

Package Description: 140 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 Emulsion with NDC 51346-064 is a product labeled by Nature Republic Co., Ltd.. The generic name of Placenta Ex Emulsion is . The product's dosage form is and is administered via form.

Labeler Name: Nature Republic Co., Ltd.

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • NIACINAMIDE (UNII: 25X51I8RD4)

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: 10-01-2012 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 - INACTIVATED, the listing data was inactivated by the FDA. 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Placenta Ex Emulsion Product Label Images

Placenta Ex Emulsion 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 1.7%

Inactive Ingredient

Inactive Ingredients:Water, Glycerin, Cetyl Ethylhexanoate, Butylene Glycol, Mineral Oil, Niacinamide, Octyldodecyl Myristate, Polysorbate 60, Cetearyl Alcohol, Petrolatum, Pentylene Glycol, Glyceryl Stearate SE, Stearic Acid, Glycine Soja (Soybean)Phytoplacenta Extract, Macadamia Integrifolia Seed Oil, Sorbitan Sesquioleate, Beeswax, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Polysorbate 80, Sorbitan Stearate, Phenoxyethanol, Fragrance (Parfum), Carbomer, Triethanolamine, 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 and wrinkle improvement.

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: After using our essence, apply an appropriate amount to the entire face.

Dosage And Administration

How to Use: After using our essence, apply an appropriate amount to the entire face.

* Please review the disclaimer below.