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  4. NDC Product Code: 50403-999 Iqqu Advance Sunscreen

NDC 50403-999 Iqqu Advance Sunscreen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50403-999?
  4. Iqqu Advance Sunscreen 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:
50403-999
Proprietary Name:
Iqqu Advance Sunscreen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Iqqu Usa Co.
Labeler Code:
50403
Product Label ID:
e35234bf-ee75-4cb6-8984-e5ed4a293696
Start Marketing Date: [9]
01-25-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 50403-999?

The NDC code 50403-999 is assigned by the FDA to the product Iqqu Advance Sunscreen which is product labeled by Iqqu Usa Co.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50403-999-92 1 tube in 1 carton / 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 Iqqu Advance Sunscreen?

Advance formula, use a small amount only. Apply evenly over clean skin until fully absorbed. Apply as needed before sun exposure.Keep the sunscreen tube away from direct sunlight to preserve its efficiency.      

Which are Iqqu Advance Sunscreen UNII Codes?

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

Which are Iqqu Advance Sunscreen 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".