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  4. NDC Product Code: 41167-0936 Act Kids Anticavity Fluoride Fruit Punch

NDC 41167-0936 Act Kids Anticavity Fluoride Fruit Punch

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 41167-0936?
  5. Act Kids Anticavity Fluoride Fruit Punch Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
41167-0936
Proprietary Name:
Act Kids Anticavity Fluoride Fruit Punch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Chattem, Inc.
Labeler Code:
41167
Product Label ID:
f21a6e6f-e1a0-4520-b29e-beaeb2f6dd1f
Start Marketing Date: [9]
12-16-2015
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PURPLE (C48327)
Flavor(s):
FRUIT PUNCH (C73390)

Code Structure Chart

Product Details

What is NDC 41167-0936?

The NDC code 41167-0936 is assigned by the FDA to the product Act Kids Anticavity Fluoride Fruit Punch which is product labeled by Chattem, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41167-0936-5 500 ml in 1 bottle, dispensing . 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 Act Kids Anticavity Fluoride Fruit Punch?

Adults and children 6 years of age and older: use once a day after brushing your teeth with a toothpasteremove caphold bottle upright and squeeze. Fill to FILL LINEpour out. Only the correct 10 milliliters dose will pour out.vigorously swish 10 milliliters of rinse between your teeth for 1 minute and then spit outdo not swallow the rinsedo not eat or drink for 30 minutes after rinsinginstruct children under 12 years of age in good rinsing habits (to minimize swallowing)supervise children as necessary until capable of using without supervisionchildren under 6 years of age: consult a dentist or doctor

Which are Act Kids Anticavity Fluoride Fruit Punch UNII Codes?

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

Which are Act Kids Anticavity Fluoride Fruit Punch 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 Act Kids Anticavity Fluoride Fruit Punch?

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: 240698 - sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse
  • RxCUI: 240698 - sodium fluoride 0.5 MG/ML Mouthwash
  • RxCUI: 656809 - ACT 0.05 % (fluoride ion 0.02 % ) Mouthwash
  • RxCUI: 656809 - sodium fluoride 0.5 MG/ML Mouthwash [ACT Fluoride Rinse]
  • RxCUI: 656809 - ACT Fluoride Rinse 0.05 % (as fluoride ion 0.02 % ) Mouthwash

* 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".