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  4. NDC Product Code: 37945-868 Pro-tect Everyday Sunscreen Spf 15

NDC 37945-868 Pro-tect Everyday Sunscreen Spf 15

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 37945-868?
  5. Pro-tect Everyday Sunscreen Spf 15 Uses
  6. Active Ingredients UNII Codes
  7. 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:
37945-868
Proprietary Name:
Pro-tect Everyday Sunscreen Spf 15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bio-medical & Pharmaceutical Manufacturing Corporation
Labeler Code:
37945
Product Label ID:
1fbe0198-177d-4e6d-a103-cc2d75ef5cbb
Start Marketing Date: [9]
12-01-1987
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Characteristics

Code Structure Chart

Product Details

What is NDC 37945-868?

The NDC code 37945-868 is assigned by the FDA to the product Pro-tect Everyday Sunscreen Spf 15 which is product labeled by Bio-medical & Pharmaceutical Manufacturing Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 37945-868-65 190 g in 1 bottle, plastic . 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 Pro-tect Everyday Sunscreen Spf 15?

•Apply liberally and evenly on all exposed areas 20-30 minutes before exposure to the sun and as needed. •Children under 6 months of age: ask a doctor.

Which are Pro-tect Everyday Sunscreen Spf 15 UNII Codes?

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

Which are Pro-tect Everyday Sunscreen Spf 15 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".