NDC 61657-0327 Hpz

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:
61657-0327
Proprietary Name:
Hpz
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
White Manufacturing Inc. Dba Micro-west
Labeler Code:
61657
Start Marketing Date: [9]
08-30-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 61657-0327-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 61657-0327?

The NDC code 61657-0327 is assigned by the FDA to the product Hpz which is product labeled by White Manufacturing Inc. Dba Micro-west. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61657-0327-1 30 ml in 1 bottle, dropper . 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 Hpz?

DIRECTIONS: Take 6 drops orally, 4 times a day. For ages 2 to adult

Which are Hpz UNII Codes?

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

Which are Hpz 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".