NDC 64471-196 Allercetin

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:
64471-196
Proprietary Name:
Allercetin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Source Naturals, Inc.
Labeler Code:
64471
Start Marketing Date: [9]
09-05-2014
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
10 MM
Imprint(s):
H
Score:
1

Product Packages

NDC Code 64471-196-48

Package Description: 7200 mg in 1 BLISTER PACK

Product Details

What is NDC 64471-196?

The NDC code 64471-196 is assigned by the FDA to the product Allercetin which is product labeled by Source Naturals, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64471-196-48 7200 mg in 1 blister pack . 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 Allercetin?

Chew 1 tablet slightly and allow to dissolve in the mouth. Adults take one every 2 to 4 hours until symptoms improve. Then take only as needed to maintain your well-being. Children ages 2 to 12 years, use one-half the adult dosage. For children under the age of 2 years, consult your health care professional.For Best Results: Keep mouth free of food and strong tastes (such as toothpaste, mouthwash and tobacco) for 15 minutes before and after taking this medicine. These substances may interfere with mucosal absorption.

Which are Allercetin UNII Codes?

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

Which are Allercetin 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:

* Please review the disclaimer below.

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".