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  4. NDC Product Code: 26052-035 Natural Acne Solutions 3 Step Regimen

NDC 26052-035 Natural Acne Solutions 3 Step Regimen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 26052-035?
  4. Natural Acne Solutions 3 Step Regimen Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
26052-035
Proprietary Name:
Natural Acne Solutions 3 Step Regimen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Burt's Bees
Labeler Code:
26052
Product Label ID:
310198a7-eb46-57e6-e054-00144ff88e88
Start Marketing Date: [9]
01-02-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 26052-035?

The NDC code 26052-035 is assigned by the FDA to the product Natural Acne Solutions 3 Step Regimen which is product labeled by Burt's Bees. The product's dosage form is . The product is distributed in a single package with assigned NDC code 26052-035-10 1 kit in 1 box * 7.5 g in 1 bottle, with applicator (26052-011-03) * 55 g in 1 bottle, pump (26052-012-01) * 145 ml in 1 bottle, plastic (26052-010-02). 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 Natural Acne Solutions 3 Step Regimen?

PENETRATES PORES TO CONTROL ACNE.HELPS PREVENT THE DEVELOPMENT OF NEW BLEMISHES

Which are Natural Acne Solutions 3 Step Regimen UNII Codes?

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

Which are Natural Acne Solutions 3 Step Regimen 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 Natural Acne Solutions 3 Step Regimen?

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: 1038982 - salicylic acid 1 % Medicated Liquid Soap
  • RxCUI: 1038982 - salicylic acid 10 MG/ML Medicated Liquid Soap
  • RxCUI: 1789221 - {1 (145 ML) (salicylic acid 10 MG/ML Medicated Liquid Soap) / 1 (60 ML) (salicylic acid 10 MG/ML Topical Lotion) / 1 (7.5 ML) (salicylic acid 7.5 MG/ML Topical Solution) } Pack
  • RxCUI: 1789221 - salicylic acid 1 % Medicated Liquid Soap (145 ML) / salicylic acid 1 % Topical Lotion (60 ML) / salicylic acid 0.75 % Topical Solution (7.5 ML) Pack
  • RxCUI: 1789221 - {1 (5 OZ) (salicylic acid 1 % Medicated Liquid Soap) / 1 (2 OZ) (salicylic acid 1 % Topical Lotion) / 1 (0.26 OZ) (salicylic acid 0.75 % Topical Solution) } Pack

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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".