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  4. NDC Product Code: 69096-8002 Linea Jose Ignacio Sunscreen Broad Spectrum Spf 30 With Zinc

NDC 69096-8002 Linea Jose Ignacio Sunscreen Broad Spectrum Spf 30 With Zinc

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 69096-8002?
  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:
69096-8002
Proprietary Name:
Linea Jose Ignacio Sunscreen Broad Spectrum Spf 30 With Zinc
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Linea Jose Ignacio Llc
Labeler Code:
69096
Product Label ID:
785e3475-ae07-1018-e053-2a91aa0a1d0a
Start Marketing Date: [9]
10-01-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Code Structure Chart

Product Details

What is NDC 69096-8002?

The NDC code 69096-8002 is assigned by the FDA to the product Linea Jose Ignacio Sunscreen Broad Spectrum Spf 30 With Zinc which is product labeled by Linea Jose Ignacio Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69096-8002-1 150 g in 1 tube , 69096-8002-2 150 g in 1 carton . 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.

Which are Linea Jose Ignacio Sunscreen Broad Spectrum Spf 30 With Zinc UNII Codes?

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

Which are Linea Jose Ignacio Sunscreen Broad Spectrum Spf 30 With Zinc 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".