NDC 59875-1015 Lab1796 Sore Throat Soothe

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59875-1015
Proprietary Name:
Lab1796 Sore Throat Soothe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Homeopathystore.com
Labeler Code:
59875
Start Marketing Date: [9]
01-01-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 59875-1015-1

Package Description: 85 PELLET in 1 TUBE

Product Details

What is NDC 59875-1015?

The NDC code 59875-1015 is assigned by the FDA to the product Lab1796 Sore Throat Soothe which is product labeled by Homeopathystore.com. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59875-1015-1 85 pellet 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.

Which are Lab1796 Sore Throat Soothe UNII Codes?

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

Which are Lab1796 Sore Throat Soothe 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".