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  4. NDC Product Code: 35617-399 Cleansing Wipe / Tube

NDC 35617-399 Cleansing Wipe / Tube

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 35617-399?
  4. Cleansing Wipe / Tube 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:
35617-399
Proprietary Name:
Cleansing Wipe / Tube
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nantong Strip Medical Supply Co.,ltd.
Labeler Code:
35617
Product Label ID:
fa9c934b-f00a-432d-9084-ce1bfdb4ec0c
Start Marketing Date: [9]
08-12-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 35617-399?

The NDC code 35617-399 is assigned by the FDA to the product Cleansing Wipe / Tube which is product labeled by Nantong Strip Medical Supply Co.,ltd.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 35617-399-01 1 pouch in 1 packet / 2 ml in 1 pouch, 35617-399-02 15 ml in 1 tube , 35617-399-03 20 ml in 1 tube , 35617-399-04 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 Cleansing Wipe / Tube?

Clean affected area

Which are Cleansing Wipe / Tube UNII Codes?

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

Which are Cleansing Wipe / Tube 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".