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  4. NDC Product Code: 29500-9181 Advanced Fluoride Anticavity

NDC 29500-9181 Advanced Fluoride Anticavity

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 29500-9181?
  4. Advanced Fluoride Anticavity Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
29500-9181
Proprietary Name:
Advanced Fluoride Anticavity
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Personal Care Products, Llc
Labeler Code:
29500
Product Label ID:
7881ff17-5188-47e6-8d2b-9c296ce35411
Start Marketing Date: [9]
07-24-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 29500-9181-6

Package Description: 1 TUBE in 1 PACKAGE / 181 g in 1 TUBE

Product Details

What is NDC 29500-9181?

The NDC code 29500-9181 is assigned by the FDA to the product Advanced Fluoride Anticavity which is product labeled by Personal Care Products, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 29500-9181-6 1 tube in 1 package / 181 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 Advanced Fluoride Anticavity?

Adults and children 2 years. and older: brush teeth thoroughly after meals or at least twice a day or as directed by a dentist.do not swallowto minimize swallowing, use a pea-sized amount in children under 6 years oldsupervise children's brushing until good habits are establishedchildren under 2y ears: ask a dentist before use.

Which are Advanced Fluoride Anticavity UNII Codes?

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

Which are Advanced Fluoride Anticavity 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:

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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".