NDC 51439-007 Acne Clearning Treatment Face

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
51439-007
Proprietary Name:
Acne Clearning Treatment Face
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Carepluss Pharma S.a. De C.v.
Labeler Code:
51439
Start Marketing Date: [9]
08-06-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51439-007-02

Package Description: 3 BOTTLE in 1 BOX / .024 mg in 1 BOTTLE (51439-007-01)

Product Details

What is NDC 51439-007?

The NDC code 51439-007 is assigned by the FDA to the product Acne Clearning Treatment Face which is product labeled by Carepluss Pharma S.a. De C.v.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51439-007-02 3 bottle in 1 box / .024 mg in 1 bottle (51439-007-01). 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 Clearning Treatment Face?

Directions:Acne Clearing CleanserAcne Clearing TonicAcne Clearing Treatment 101

Which are Acne Clearning Treatment Face UNII Codes?

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

Which are Acne Clearning Treatment Face 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:

What is the NDC to RxNorm Crosswalk for Acne Clearning Treatment Face?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1372925 - {1 (240 ML) (benzoyl peroxide 25 MG/ML Medicated Liquid Soap) / 1 (120 ML) (salicylic acid 20 MG/ML Topical Solution) / 1 (60 ML) (sulfur 50 MG/ML Topical Solution) } Pack
  • RxCUI: 1372925 - benzoyl peroxide 2.5 % Medicated Liquid Soap (240 ML) / salicylic acid 2 % Topical Solution (120 ML) / sulfur 5 % Topical Solution (60 ML) Pack
  • RxCUI: 1372925 - {1 (240 ML) (benzoyl peroxide 2.5 % Medicated Liquid Soap) / 1 (120 ML) (salicylic acid 2 % Topical Solution) / 1 (60 ML) (sulfur 5 % Topical Solution) } Pack
  • RxCUI: 251577 - salicylic acid 2 % Topical Solution
  • RxCUI: 251577 - salicylic acid 20 MG/ML Topical Solution

* 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".