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NDC 70773-100 Tonsin

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 70773-100?
  5. Tonsin 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:
70773-100
Proprietary Name:
Tonsin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Private Label Brands Cc
Labeler Code:
70773
Product Label ID:
6157d00e-9893-6038-e053-2a91aa0ab6e6
Start Marketing Date: [9]
12-25-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
8 MM
Score:
1

Code Structure Chart

Product Details

What is NDC 70773-100?

The NDC code 70773-100 is assigned by the FDA to the product Tonsin which is product labeled by Private Label Brands Cc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70773-100-15 1 bottle in 1 carton / 1 [hp_x] 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 Tonsin?

Adults and children aged 12 years or older:Dissolve 2 tablets in mouth 3x daily. May be taken hourly in acute casesChildren between 2 and 12 years old:Dissolve 1 tablet in mouth 3x daily. May be taken hourly in acute cases.Infants: 1 crushed tablet diluted in cooled, boiled, water.

Which are Tonsin UNII Codes?

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

Which are Tonsin 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".