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  4. NDC Product Code: 58892-118 Cotz Spf 35 Sunscreen

NDC 58892-118 Cotz Spf 35 Sunscreen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 58892-118?
  4. Cotz Spf 35 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:
58892-118
Proprietary Name:
Cotz Spf 35 Sunscreen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Fallien Cosmeceuticals, Ltd.
Labeler Code:
58892
Product Label ID:
47d076f6-df6b-4b76-afb5-f8d56b577f93
Start Marketing Date: [9]
03-01-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 58892-118?

The NDC code 58892-118 is assigned by the FDA to the product Cotz Spf 35 Sunscreen which is product labeled by Fallien Cosmeceuticals, Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58892-118-01 1 tube in 1 carton / 100 g 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 Cotz Spf 35 Sunscreen?

Apply generously and uniformly to all exposed skin areas before exposure to sunlight Continue to rub in until fading occurs, especially in hair bearing areas Reapply as needed and after washing, swimming, towel drying, or sweating for maximum protection. Other InformationSun Alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun. May stain some fabrics

Which are Cotz Spf 35 Sunscreen UNII Codes?

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

Which are Cotz Spf 35 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".