NDC 72543-030 Jdew Green Moist

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72543-030
Proprietary Name:
Jdew Green Moist
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
J'ers Co.,ltd
Labeler Code:
72543
Start Marketing Date: [9]
08-01-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72543-030-02

Package Description: 1 CONTAINER in 1 CARTON / 130 mL in 1 CONTAINER (72543-030-01)

Product Details

What is NDC 72543-030?

The NDC code 72543-030 is assigned by the FDA to the product Jdew Green Moist which is product labeled by J'ers Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72543-030-02 1 container in 1 carton / 130 ml in 1 container (72543-030-01). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Jdew Green Moist?

Directions:After toner and essence, apply 2-3 pumps of the lotion on your face, outwards from the center of your face.

Which are Jdew Green Moist UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Jdew Green Moist Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".