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  4. NDC Product Code: 34331-302 Migrapure

NDC 34331-302 Migrapure

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 34331-302?
  5. Migrapure 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:
34331-302
Proprietary Name:
Migrapure
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Puramed Bioscience, Inc.
Labeler Code:
34331
Product Label ID:
3595fe4f-1b85-4c27-aa22-912a27159055
Start Marketing Date: [9]
01-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
PEPPERMINT (C73408 - PEPPERMINT)

Code Structure Chart

Product Details

What is NDC 34331-302?

The NDC code 34331-302 is assigned by the FDA to the product Migrapure which is product labeled by Puramed Bioscience, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 34331-302-04 4 dose pack in 1 box / 3 ml in 1 dose 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 Migrapure?

To open UnitDose dispenser, tear off the perforated end. Squeeze entire contents under the tongue. Important: Hold gel under the tongue for 60 seconds, then swallow.Repeat after 5 minutes using a second UnitDose dispenser.Avoid eating or drinking liquids for 15 minutes after each dose.An additional dose may be taken after 30 minutes. Take 1 or 2 UnitDose dispensers, as needed or as directed by a doctor

Which are Migrapure UNII Codes?

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

Which are Migrapure 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".