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  4. NDC Product Code: 71167-005 Plak Smacker Anti-cavity Fluoride Gel

NDC 71167-005 Plak Smacker Anti-cavity Fluoride Gel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71167-005?
  4. Plak Smacker Anti-cavity Fluoride Gel 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:
71167-005
Proprietary Name:
Plak Smacker Anti-cavity Fluoride Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Huaian Zongheng Bio-tech Co., Ltd
Labeler Code:
71167
Product Label ID:
6657b534-f79a-0407-e053-2a91aa0a0f45
Start Marketing Date: [9]
02-02-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 71167-005?

The NDC code 71167-005 is assigned by the FDA to the product Plak Smacker Anti-cavity Fluoride Gel which is product labeled by Huaian Zongheng Bio-tech Co., Ltd. The product's dosage form is . The product is distributed in 13 packages with assigned NDC codes 71167-005-01 144 tube in 1 carton / 24 g in 1 tube, 71167-005-02 120 box in 1 carton / 24 tube in 1 box / 28 g in 1 tube, 71167-005-03 120 box in 1 carton / 24 tube in 1 box / 120 g in 1 tube, 71167-005-04 144 tube in 1 carton / 50 g in 1 tube, 71167-005-05 72 tube in 1 carton / 100 g in 1 tube, 71167-005-06 144 tube in 1 box / 100 g in 1 tube, 71167-005-07 480 tube in 1 box / 28 g in 1 tube, 71167-005-08 72 tube in 1 box / 120 g in 1 tube, 71167-005-09 144 tube in 1 box / 120 g in 1 tube, 71167-005-10 288 tube in 1 box / 50 g in 1 tube, 71167-005-11 480 box in 1 carton / 24 tube in 1 box / 28 g in 1 tube, 71167-005-12 576 box in 1 carton / 144 tube in 1 box / 24 g in 1 tube, 71167-005-13 72 box in 1 carton / 12 tube in 1 box / 120 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 Plak Smacker Anti-cavity Fluoride Gel?

Adults and children 6 years of age and older:brush teeth thoroughly, after meals or at least twice a day or use as directed by a dentist.do not swallowto minimize swallowing use a pea-sized amount in children under 6supervise children as necessary until capable of using without supervision

Which are Plak Smacker Anti-cavity Fluoride Gel UNII Codes?

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

Which are Plak Smacker Anti-cavity Fluoride Gel 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 Plak Smacker Anti-cavity Fluoride Gel?

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.

[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".