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  4. NDC Product Code: 53634-125 Acne Treatment Daytime

NDC 53634-125 Acne Treatment Daytime

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 53634-125?
  4. Acne Treatment Daytime 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:
53634-125
Proprietary Name:
Acne Treatment Daytime
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Malin And Goetz Inc
Labeler Code:
53634
Product Label ID:
61ce6585-0cde-4d21-84b8-f37a95327605
Start Marketing Date: [9]
01-03-2018
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 53634-125-02

Package Description: 1 PACKAGE in 1 CARTON / 15 mL in 1 PACKAGE (53634-125-01)

Product Details

What is NDC 53634-125?

The NDC code 53634-125 is assigned by the FDA to the product Acne Treatment Daytime which is product labeled by Malin And Goetz Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53634-125-02 1 package in 1 carton / 15 ml in 1 package (53634-125-01). 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 Acne Treatment Daytime?

Using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin. If this occurs, only one drug should  be used, unless directed by a doctor

Which are Acne Treatment Daytime UNII Codes?

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

Which are Acne Treatment Daytime 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".