NDC 51596-010 Headache Relief To Go

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:
51596-010
Proprietary Name:
Headache Relief To Go
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Breakthrough Products Inc.
Labeler Code:
51596
Start Marketing Date: [9]
07-15-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
ORANGE (C73406)

Product Packages

NDC Code 51596-010-01

Package Description: 1 POWDER in 1 POUCH

Product Details

What is NDC 51596-010?

The NDC code 51596-010 is assigned by the FDA to the product Headache Relief To Go which is product labeled by Breakthrough Products Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51596-010-01 1 powder in 1 pouch . 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 Headache Relief To Go?

Do not take more than directed (see overdose warning)adults and children 12 years and oversee instructions above for opening packetplace 1 powder on the tongue and swallow with or without waterrepeat every 4-6 hours, wile symptoms persistdo not take more than 6 pouches in 24 hourschildren under 12 years: ask a doctor

Which are Headache Relief To Go UNII Codes?

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

Which are Headache Relief To Go 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:

What is the NDC to RxNorm Crosswalk for Headache Relief To Go?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".