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NDC 73134-040 Unpa Cha Cha Toothpaste

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73134-040?
  4. Unpa Cha Cha Toothpaste 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:
73134-040
Proprietary Name:
Unpa Cha Cha Toothpaste
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lycl Inc.
Labeler Code:
73134
Product Label ID:
123d1e02-87b8-45d2-90f8-4b83675e526f
Start Marketing Date: [9]
02-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 73134-040?

The NDC code 73134-040 is assigned by the FDA to the product Unpa Cha Cha Toothpaste which is product labeled by Lycl Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73134-040-02 1 tube in 1 carton / 100 g in 1 tube (73134-040-01). 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 Unpa Cha Cha Toothpaste?

■ Brushing the teeth with a suitable amount

Which are Unpa Cha Cha Toothpaste UNII Codes?

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

Which are Unpa Cha Cha Toothpaste 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 Unpa Cha Cha Toothpaste?

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".