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  4. NDC Product Code: 0135-0432 Aquafresh Extreme Clean Deep Action

NDC 0135-0432 Aquafresh Extreme Clean Deep Action

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 0135-0432?
  4. Aquafresh Extreme Clean Deep Action 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 .
NDC Product Code:
0135-0432
Proprietary Name:
Aquafresh Extreme Clean Deep Action
Product Type: [3]
Labeler Name: [5]
Haleon Us Holdings Llc
Labeler Code:
0135
Product Label ID:
aaff19d9-4ba5-462a-893b-7220feb25d6c
FDA Application Number: [6]
M022
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
03-25-2011
End Marketing Date: [10]
07-31-2019
Listing Expiration Date: [11]
07-31-2019
Exclude Flag: [12]
D
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Product Details

What is NDC 0135-0432?

The NDC code 0135-0432 is assigned by the FDA to the product Aquafresh Extreme Clean Deep Action which is product labeled by Haleon Us Holdings Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 0135-0432-02 1 tube in 1 carton / 158.7 g in 1 tube, 0135-0432-05 1 tube in 1 carton / 22.7 g in 1 tube. 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 Aquafresh Extreme Clean Deep Action?

•adults and children 2 years and older:•apply toothpaste onto a toothbrush •brush teeth thoroughly, preferably after each meal, or at least twice a day, and not more than 3 times a day, or as directed by a dentist or doctor. Minimize swallowing. Spit out after brushing.•to minimize swallowing for children under 6 years of age, use a pea-sized amount and supervise brushing and rinsing until good habits are established•children under 2 years consult a dentist or doctor

Which are Aquafresh Extreme Clean Deep Action UNII Codes?

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

Which are Aquafresh Extreme Clean Deep Action 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 Aquafresh Extreme Clean Deep Action?

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:

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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.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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.

[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

[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".