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  4. NDC Product Code: 73306-1138 Above Women Derma Clinical 72 H

NDC 73306-1138 Above Women Derma Clinical 72 H

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 73306-1138?
  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:
73306-1138
Proprietary Name:
Above Women Derma Clinical 72 H
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Baston Industria De Aerossois Ltda
Labeler Code:
73306
Product Label ID:
ed786876-9d6a-521f-e053-2a95a90ad0f6
Start Marketing Date: [9]
11-14-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 73306-1138-1

Package Description: 50 g in 1 BOTTLE, PLASTIC

Product Details

What is NDC 73306-1138?

The NDC code 73306-1138 is assigned by the FDA to the product Above Women Derma Clinical 72 H which is product labeled by Baston Industria De Aerossois Ltda. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73306-1138-1 50 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.

Which are Above Women Derma Clinical 72 H UNII Codes?

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

  • ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M)
  • ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (Active Moiety)

Which are Above Women Derma Clinical 72 H 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".