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  4. NDC Product Code: 41900-200 Quik Gel

NDC 41900-200 Quik Gel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 41900-200?
  4. Quik Gel 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:
41900-200
Proprietary Name:
Quik Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cinogen Cosmetics Zhaoqing, Ltd.
Labeler Code:
41900
Product Label ID:
4c499b0c-a2d5-48f1-bc42-226c075d17b8
Start Marketing Date: [9]
10-01-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 41900-200-02

Package Description: 10 PACKET in 1 BAG / 1.28 g in 1 PACKET (41900-200-01)

Product Details

What is NDC 41900-200?

The NDC code 41900-200 is assigned by the FDA to the product Quik Gel which is product labeled by Cinogen Cosmetics Zhaoqing, Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41900-200-02 10 packet in 1 bag / 1.28 g in 1 packet (41900-200-01). 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 Quik Gel?

DirectionsWet hands thoroughly with product and allow to dry without wiping.For children under 6, use only only under adult supervision.

Which are Quik Gel UNII Codes?

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

Which are Quik Gel 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:

* Please review the disclaimer below.

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".