NDC 51596-008 Ache And Pain 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:
51596-008
Proprietary Name:
Ache And Pain Relief To Go
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
51596
Start Marketing Date: [9]
10-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
LEMON (C73396 - LEMON-LIME)

Code Structure Chart

Product Details

What is NDC 51596-008?

The NDC code 51596-008 is assigned by the FDA to the product Ache And Pain Relief To Go which is product labeled by Breakthrough Products Inc.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 51596-008-01 1 powder in 1 pouch , 51596-008-05 5 pouch in 1 box / 1 powder in 1 pouch (51596-008-01), 51596-008-10 10 packet in 1 box / 1 powder in 1 packet, 51596-008-12 12 pouch in 1 box / 1 powder in 1 pouch (51596-008-01), 51596-008-24 24 pouch in 1 box / 1 powder in 1 pouch (51596-008-01). 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 Ache And Pain Relief To Go?

Adults and children 12 years and over:see instructions in red box for opening packetplace 1 powder on the tongue and swallow with or without waterrepeat every 4-6 hours, while symptoms persistdo not take more than 4 powders in 24 hourschildren under 12 years: ask a doctor

Which are Ache And Pain Relief To Go UNII Codes?

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

Which are Ache And Pain 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 Ache And Pain 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:

* 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".