NDC 44597-5358 Herbon Wild Cherry

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:
44597-5358
Proprietary Name:
Herbon Wild Cherry
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Purity Life Division Of Sunopta
Labeler Code:
44597
Start Marketing Date: [9]
09-30-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
Shape:
OVAL (C48345)
Size(s):
23 MM
Imprint(s):
E
Score:
1
Flavor(s):
CHERRY (C73375 - WILD CHERRY)

Product Packages

NDC Code 44597-5358-0

Package Description: 12 CELLO PACK in 1 CARTON / 18 LOZENGE in 1 CELLO PACK

Product Details

What is NDC 44597-5358?

The NDC code 44597-5358 is assigned by the FDA to the product Herbon Wild Cherry which is product labeled by Purity Life Division Of Sunopta. The product's dosage form is . The product is distributed in a single package with assigned NDC code 44597-5358-0 12 cello pack in 1 carton / 18 lozenge in 1 cello 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 Herbon Wild Cherry?

Adults and children 3 years of age and older: allow lozenge to dissolve slowly in the mouth. May be repeated every 2 hours as needed or as directed by a physician. Children under 3 years of age: consult a physician.

Which are Herbon Wild Cherry UNII Codes?

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

Which are Herbon Wild Cherry 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".