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  4. NDC Product Code: 66894-0000 Country Gent

NDC 66894-0000 Country Gent

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 66894-0000?
  5. Country Gent Uses
  6. Active Ingredients UNII Codes
  7. 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:
66894-0000
Proprietary Name:
Country Gent
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Heavenly Harvest, Inc.
Labeler Code:
66894
Product Label ID:
b0a72b13-14a5-4086-a05c-6c9a515374ce
Start Marketing Date: [9]
01-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
PEPPERMINT (C73408)

Code Structure Chart

Product Details

What is NDC 66894-0000?

The NDC code 66894-0000 is assigned by the FDA to the product Country Gent which is product labeled by Heavenly Harvest, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66894-0000-1 113 g in 1 bottle . 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 Country Gent?

Adults and Children 6 years of age & older: Apply powder to wet toothbrush; completely cover bristles. Brush 30 seconds. Reapply powder as before and brush again. Rinse and expel thoroughly. Brush teeth, after each meal or at least twice a day, or as directed by a dentist or doctor. Instruct children under 12 years of age in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision.  Children under 6 years of age: Do not use unless directed by a dentist or doctor.

Which are Country Gent UNII Codes?

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

Which are Country Gent 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".