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  4. NDC Product Code: 70798-415 Zinc Oxide, Titanium Dioxide

NDC 70798-415 Zinc Oxide, Titanium Dioxide

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70798-415?
  4. Zinc Oxide, Titanium Dioxide 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:
70798-415
Proprietary Name:
Zinc Oxide, Titanium Dioxide
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Matchco Inc.
Labeler Code:
70798
Product Label ID:
32aa75a5-49b3-35ab-e054-00144ff88e88
Start Marketing Date: [9]
07-11-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 70798-415?

The NDC code 70798-415 is assigned by the FDA to the product Zinc Oxide, Titanium Dioxide which is product labeled by Matchco Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70798-415-22 30 g in 1 bottle, glass . 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 Zinc Oxide, Titanium Dioxide?

Useshelps prevent sunburnhigher SPF gives more sunburn protectionWarningsFor external use onlyDo not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Which are Zinc Oxide, Titanium Dioxide UNII Codes?

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

Which are Zinc Oxide, Titanium Dioxide 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".