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  4. NDC Product Code: 73020-060 Papa Recipe Eggplant Clearing

NDC 73020-060 Papa Recipe Eggplant Clearing

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73020-060?
  4. Papa Recipe Eggplant Clearing Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
73020-060
Proprietary Name:
Papa Recipe Eggplant Clearing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Costory Co., Ltd
Labeler Code:
73020
Product Label ID:
46309e70-0348-4953-bcc5-886c30057e76
Start Marketing Date: [9]
03-01-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 73020-060?

The NDC code 73020-060 is assigned by the FDA to the product Papa Recipe Eggplant Clearing which is product labeled by Costory Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73020-060-02 1 container in 1 carton / 50 ml in 1 container (73020-060-01). 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 Papa Recipe Eggplant Clearing?

Directions■ After ritual cleansing and toning, pre-moisten your skin with any lightweight emulsion followed by essence or serum.■ Apply to the face daily, morning & night, massaging the cream in outward sweeping motions from the center of your face.■ Gently pat the remaining cream until fully absorbed into skin.

Which are Papa Recipe Eggplant Clearing UNII Codes?

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

Which are Papa Recipe Eggplant Clearing 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".