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  4. NDC Product Code: 71588-0011 K Oxiderm Op Post Procedure Skin Care Bruise

NDC 71588-0011 K Oxiderm Op Post Procedure Skin Care Bruise

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71588-0011?
  4. K Oxiderm Op Post Procedure Skin Care Bruise 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:
71588-0011
Proprietary Name:
K Oxiderm Op Post Procedure Skin Care Bruise
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ezekielcosmetic Co., Ltd
Labeler Code:
71588
Product Label ID:
578be57e-cee2-6ec6-e053-2991aa0aba1a
Start Marketing Date: [9]
08-17-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

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Product Details

What is NDC 71588-0011?

The NDC code 71588-0011 is assigned by the FDA to the product K Oxiderm Op Post Procedure Skin Care Bruise which is product labeled by Ezekielcosmetic Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71588-0011-1 30 ml in 1 tube . 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 K Oxiderm Op Post Procedure Skin Care Bruise?

For 4~5 days before cosmetic application, apply thinly twice a day, morning and night, after cleansing the skinapply K oxiderm OP cream right after cosmetic applicationK oxiderm OP cream is recommended for 10 to 15 days as preparatory skin care before and after surgical and medical cosmetic procedure

Which are K Oxiderm Op Post Procedure Skin Care Bruise UNII Codes?

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

Which are K Oxiderm Op Post Procedure Skin Care Bruise 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".