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  4. NDC Product Code: 29565-400 Sunscreen Sport Spf30 Plus Broad Spectrum

NDC 29565-400 Sunscreen Sport Spf30 Plus Broad Spectrum

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 29565-400?
  4. Sunscreen Sport Spf30 Plus Broad Spectrum 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:
29565-400
Proprietary Name:
Sunscreen Sport Spf30 Plus Broad Spectrum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Uv Natural International Pty Ltd
Labeler Code:
29565
Product Label ID:
b199e5cf-9b73-4b48-ae14-6d6d41c7cd03
Start Marketing Date: [9]
01-01-2006
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 29565-400-40

Package Description: 130 mL in 1 TUBE

Product Details

What is NDC 29565-400?

The NDC code 29565-400 is assigned by the FDA to the product Sunscreen Sport Spf30 Plus Broad Spectrum which is product labeled by Uv Natural International Pty Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 29565-400-40 130 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 Sunscreen Sport Spf30 Plus Broad Spectrum?

UsesHelps prevent sunburnIf used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Which are Sunscreen Sport Spf30 Plus Broad Spectrum UNII Codes?

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

Which are Sunscreen Sport Spf30 Plus Broad Spectrum 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".