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NDC 0363-3226 3 Step Acne System Well At Walgreens

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 0363-3226?
  4. 3 Step Acne System Well At Walgreens 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:
0363-3226
Proprietary Name:
3 Step Acne System Well At Walgreens
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Walgreens
Labeler Code:
0363
Product Label ID:
eddc5d88-7812-49f6-b1c0-a12230e2528c
Start Marketing Date: [9]
07-15-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 0363-3226?

The NDC code 0363-3226 is assigned by the FDA to the product 3 Step Acne System Well At Walgreens which is product labeled by Walgreens. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0363-3226-07 1 kit in 1 kit * 120 ml in 1 bottle (0363-3227-04) * 60 ml in 1 bottle (0363-3228-02). 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 3 Step Acne System Well At Walgreens?

Use morning and night. Apply a small (dime-sized) amount to dampened skin and gently massage. Rinse thoroughly with warm water. If bothersome dryness or peeling occurs, reduce application use. Follow with Refreshing Toner. • Cleans the skin thoroughly before applying medication • Cover the entire affected area one to three times a day •  Excessive drying of the skin may occur. Start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor. If bothersome dryness or peeling occurs, reduce application to once a day or every other day. • If going outside, use a sunscreen.  If sensitivity develops, discontinue use of both products and consult a doctor.

Which are 3 Step Acne System Well At Walgreens UNII Codes?

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

Which are 3 Step Acne System Well At Walgreens 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 3 Step Acne System Well At Walgreens?

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: 1600267 - {1 (120 ML) (benzoyl peroxide 25 MG/ML Medicated Liquid Soap) / 1 (60 ML) (benzoyl peroxide 25 MG/ML Topical Lotion) } Pack
  • RxCUI: 1600267 - benzoyl peroxide 2.5 % / 2.5 % Topical Kit
  • RxCUI: 1600267 - {1 (120 ML) (benzoyl peroxide 2.5 % Medicated Liquid Soap) / 1 (60 ML) (benzoyl peroxide 2.5 % Topical Lotion) } Pack
  • RxCUI: 200009 - benzoyl peroxide 2.5 % Topical Lotion
  • RxCUI: 200009 - benzoyl peroxide 25 MG/ML Topical Lotion

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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".