1. Home
  2. Labeler Index
  3. Norwood Packaging Ltd.
  4. NDC Product Code: 55143-103 Badger Spf 34 Anti-bug Sunscreen

NDC 55143-103 Badger Spf 34 Anti-bug Sunscreen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 55143-103?
  4. Badger Spf 34 Anti-bug 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:
55143-103
Proprietary Name:
Badger Spf 34 Anti-bug Sunscreen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Norwood Packaging Ltd.
Labeler Code:
55143
Product Label ID:
d9aa07df-c4df-412c-a7f9-321b6f58c0a1
Start Marketing Date: [9]
01-01-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 55143-103?

The NDC code 55143-103 is assigned by the FDA to the product Badger Spf 34 Anti-bug Sunscreen which is product labeled by Norwood Packaging Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55143-103-01 87 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 Badger Spf 34 Anti-bug Sunscreen?

For full protection, apply liberally (2mg/cm2 of skin) to all exposed skin 15 minutes before sun exposure, then rub in to reduce whitening effect.

Which are Badger Spf 34 Anti-bug Sunscreen UNII Codes?

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

Which are Badger Spf 34 Anti-bug 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:

* Please review the disclaimer below.

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".