NDC 34331-202 Lipigesic M

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:
34331-202
Proprietary Name:
Lipigesic M
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
34331
Start Marketing Date: [9]
08-08-2011
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 34331-202?

The NDC code 34331-202 is assigned by the FDA to the product Lipigesic M 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 34331-202-06 8 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 Lipigesic M?

For maximum effectiveness, begin treatment at first sign of headache.Open one unit dose dispenser by tearing off the perforated end and dispensing entire contents under the tongue.Important: Hold in place under the tongue for at least 60 seconds; then swallow. Repeat after 5 minutes using a second unit dose dispenser, hold the second dose under the tongue for at least 60 seconds before swallowing. Additional medication may be taken after 30 minutes, either I or 2 unit dose dispensers, as needed or as directed by doctor.

Which are Lipigesic M UNII Codes?

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

Which are Lipigesic M 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".