NDC 72160-0002 Wine Gold Serum

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:
72160-0002
Proprietary Name:
Wine Gold Serum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Inano Co., Ltd.
Labeler Code:
72160
Start Marketing Date: [9]
03-12-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72160-0002-1

Package Description: 10 mL in 1 BOTTLE

Product Details

What is NDC 72160-0002?

The NDC code 72160-0002 is assigned by the FDA to the product Wine Gold Serum which is product labeled by Inano Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72160-0002-1 10 ml in 1 bottle . 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 Wine Gold Serum?

[for use with mask sheet]1. after washing, remove moisture entirely to arrange skin texture2. apply the wine gold serum (step 1) onto the face equaly and rub the serum softly like massae to absorb perfectly3. unfolding the mask (step 2), position the mask on the fact according to position of eyes and mouth4. remove the mask sheet after 15~30 minutes, after that softly pat any remaining essence into skin like massage[for scalp care]apply proper amount to the scalp

Which are Wine Gold Serum UNII Codes?

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

Which are Wine Gold Serum 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".