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NDC 80905-001 Benchmarks Derma Shield

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 80905-001?
  5. Benchmarks Derma Shield 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:
80905-001
Proprietary Name:
Benchmarks Derma Shield
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Star Colour Laboratories
Labeler Code:
80905
Product Label ID:
a2d586e2-352e-4fea-a95e-85b089f1dda3
Start Marketing Date: [9]
10-09-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 80905-001?

The NDC code 80905-001 is assigned by the FDA to the product Benchmarks Derma Shield which is product labeled by Star Colour Laboratories. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 80905-001-01 57 g in 1 can , 80905-001-02 170 g in 1 can , 80905-001-03 482 g in 1 can . 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 Benchmarks Derma Shield?

Apply as neededChildren under 6 months: ask a doctorWash and dry skin areaShake can vigorouslyInvert can and apply "golf ball" sized amount in palmRub thoroughly onto the skinAllow to dry

Which are Benchmarks Derma Shield UNII Codes?

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

Which are Benchmarks Derma Shield 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".