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  4. NDC Product Code: 70749-020 Znsp Repair

NDC 70749-020 Znsp Repair

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70749-020?
  4. Znsp Repair 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:
70749-020
Proprietary Name:
Znsp Repair
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Z-ton Es Bio Co., Ltd.
Labeler Code:
70749
Product Label ID:
db887b99-5516-4754-8df5-ddca082d9a17
Start Marketing Date: [9]
05-01-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 70749-020?

The NDC code 70749-020 is assigned by the FDA to the product Znsp Repair which is product labeled by Z-ton Es Bio Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70749-020-02 10 bottle in 1 carton / 8 g in 1 bottle (70749-020-01). 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 Znsp Repair?

Indications & usage:1. After treatment and in case of irritation, apply an appropriate amount on the skin and help the penetration with massage.

Which are Znsp Repair UNII Codes?

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

Which are Znsp Repair 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".