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  4. NDC Product Code: 76445-1555 Clear-n-smooth

NDC 76445-1555 Clear-n-smooth

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 76445-1555?
  5. Clear-n-smooth 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:
76445-1555
Proprietary Name:
Clear-n-smooth
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hawknad Manufacturing Industries
Labeler Code:
76445
Product Label ID:
8e503af8-1013-8c8a-e053-2995a90aeb92
Start Marketing Date: [9]
01-02-1992
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 76445-1555?

The NDC code 76445-1555 is assigned by the FDA to the product Clear-n-smooth which is product labeled by Hawknad Manufacturing Industries. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76445-1555-6 176 g in 1 bottle, dispensing . 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 Clear-n-smooth?

Lightens dark colorations in the skin such as freckles, age, and liver spotsContains a sunscreen to help prevent darkening from re-occurring.

Which are Clear-n-smooth UNII Codes?

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

Which are Clear-n-smooth 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".