NDC 69142-020 Organic Night Repair Ampoule

NDC Product Code 69142-020

NDC 69142-020-02

Package Description: 1 CONTAINER in 1 CARTON > 45 mL in 1 CONTAINER (69142-020-01)

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

NDC Product Information

Organic Night Repair Ampoule with NDC 69142-020 is a product labeled by Yeojaya. The generic name of Organic Night Repair Ampoule is . The product's dosage form is and is administered via form.

Labeler Name: Yeojaya

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.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)

Product Labeler Information

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

Labeler Name: Yeojaya
Labeler Code: 69142
Start Marketing Date: 08-01-2018 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: 12-31-2019 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.

Organic Night Repair Ampoule Product Label Images

Organic Night Repair Ampoule 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 ingredients: Niacinamide 2.5%, Adenosine 0.1%

Inactive Ingredient

Inactive ingredients:Aloe Barbadensis Leaf Water, Sodium Hyaluronate, Butylene Glycol, Glycerin, Palmitoyl Pentapeptide-4, Glyceryl Glucoside, 1,2-Hexanediol, rh-Oligopeptide-1, Trehalose, Polysorbate 20, Sorbitol, Arginine, Petroselinum Sativum (Parsley) Extract, Cucumis Sativus (Cucumber) Fruit Extract, Althaea Officinalis Root Extract, Centaurea Cyanus Flower Extract, Citrus Limon (Lemon) Fruit Extract, Red Ginseng Extract, Calendula Officinalis Flower Extract, Caprylyl Glycol, Illicium Verum (Anise) Fruit Extract, Pearl Powder, Fragrance, Ceramide NP

Purpose

Purpose: Skin Brightening, Anti wrinkle

Warnings

Warnings:- For external use only- Avoid contact with eyes.- Discontinue use if signs of irritation or rashes appear.- Replace the cap after use.- Keep out of reach of children

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Uses

Uses:- Helps improve skin brightening- Helps improve Anti wrinkle

Directions

Directions:- After cleansing, apply appropriate amount on skin and absorb gently into skin.

* Please review the disclaimer below.