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  4. NDC Product Code: 71471-269 Aqua Plus Acne Treatment System

NDC 71471-269 Aqua Plus Acne Treatment System

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71471-269?
  4. Aqua Plus Acne Treatment System 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:
71471-269
Proprietary Name:
Aqua Plus Acne Treatment System
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Totally Clear Products, Inc
Labeler Code:
71471
Product Label ID:
2774453d-170e-4dca-96e2-60bdee79d28a
Start Marketing Date: [9]
09-01-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71471-269-27

Package Description: 1 KIT in 1 BOX * 30 mL in 1 BOTTLE (71471-312-27) * 50 mL in 1 BOTTLE (71471-416-27) * 50 mL in 1 BOTTLE (71471-561-27)

Product Details

What is NDC 71471-269?

The NDC code 71471-269 is assigned by the FDA to the product Aqua Plus Acne Treatment System which is product labeled by Totally Clear Products, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71471-269-27 1 kit in 1 box * 30 ml in 1 bottle (71471-312-27) * 50 ml in 1 bottle (71471-416-27) * 50 ml in 1 bottle (71471-561-27). 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 Aqua Plus Acne Treatment System?

Wet your skin and massage the Aqua+ Daily Cleanser over your entire face, avoiding your eyes. Use the Aqua+ Daily Cleanser only once a day until your skin acclimates, after which you can move to twice-per-day applications. Rinse with water and gently pat your skin with a clean towel. Clean the skin thoroughly before applying the Aqua+ Spotter Gel. Cover the entire affected area with a thin layer, one to three times daily. Because 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.

Which are Aqua Plus Acne Treatment System UNII Codes?

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

Which are Aqua Plus Acne Treatment System 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 Aqua Plus Acne Treatment System?

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: 1047362 - salicylic acid 1 % Topical Solution
  • RxCUI: 1047362 - salicylic acid 10 MG/ML Topical Solution
  • RxCUI: 1943754 - {1 (30 ML) (salicylic acid 0.015 MG/MG Topical Gel) / 1 (50 ML) (salicylic acid 10 MG/ML Topical Solution) / 1 (50 ML) (salicylic acid 20 MG/ML Medicated Liquid Soap) } Pack
  • RxCUI: 1943754 - salicylic acid 1 % Topical Solution (50 mL) / salicylic acid 1.5 % Topical Gel (30 mL) / salicylic acid 2 % Medicated Liquid Soap (50 mL) Pack
  • RxCUI: 1943754 - salicylic acid 1 % Topical Solution (50 ML) / salicylic acid 1.5 % Topical Gel (30 ML) / salicylic acid 2 % Medicated Liquid Soap (50 ML) Pack

* 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".