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  4. NDC Product Code: 70230-1001 Medi All 4 Cleanser (niacinamide)

NDC 70230-1001 Medi All 4 Cleanser (niacinamide)

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70230-1001?
  4. Medi All 4 Cleanser (niacinamide) 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:
70230-1001
Proprietary Name:
Medi All 4 Cleanser (niacinamide)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Katecosmetics. Co., Ltd, (kisd)
Labeler Code:
70230
Product Label ID:
31983126-5db1-0162-e054-00144ff88e88
Start Marketing Date: [9]
04-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 70230-1001?

The NDC code 70230-1001 is assigned by the FDA to the product Medi All 4 Cleanser (niacinamide) which is product labeled by Katecosmetics. Co., Ltd, (kisd). The product's dosage form is . The product is distributed in a single package with assigned NDC code 70230-1001-1 500 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 Medi All 4 Cleanser (niacinamide)?

Avoid contact with the eyes. In case of accidental contact, rinse eyes with large amounts of cool tap water.

Which are Medi All 4 Cleanser (niacinamide) UNII Codes?

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

Which are Medi All 4 Cleanser (niacinamide) 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".