Brioschi Effervescent Antacid
NDC 69276-200

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 69276-200?
  5. Brioschi Effervescent Antacid Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Brioschi Effervescent Antacid is a OTC MONOGRAPH FINAL-approved product labeled by Neobourne Pharma Lp. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a white product. This product entry covers the primary NDC 69276-200 and 5 associated package configurations. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
69276-200
Proprietary Name:
Brioschi Effervescent Antacid
Product Type: [3]
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Neobourne Pharma Lp
Labeler Code:
69276
Product Label ID:
513e0139-2666-07cb-e054-00144ff8d46c
FDA Application Number: [6]
part331
Marketing Category: [8]
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.

Marketing Timeline

Start Marketing Date: [9]
06-30-2015
End Marketing Date: [10]
02-04-2016
Listing Expiration Date: [11]
02-04-2016
Exclude Flag: [12]
D

Product Characteristics

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

Code Structure Chart

Product Details

What is NDC 69276-200?

The NDC code 69276-200 is assigned by the FDA to the product Brioschi Effervescent Antacid. This pharmaceutical product is labeled by Neobourne Pharma Lp and is currently categorized as listed product. In terms of distribution, this product is available in 5 different package configurations. The associated package NDC(s) include: 69276-200-05, 69276-200-10, 69276-200-24, 69276-200-25, 69276-200-58. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Fully dissolve 5 grams (1 packet) in a 4-6 ounces of water before drinking • do not use more than directedAdults and children 12 years and olderAdults 60 years and olderChildren under 12One dose (1 packet) each hourOne dose (1 packet) each hourAsk a doctorDo not exceed 4 doses in 24 hoursDo not exceed 4 doses in 24 hours

Which are the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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 this product?

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:
  • RxCUI: 1656654 - sodium bicarbonate 1.02 GM per 5 GM Granules for Oral Solution
  • RxCUI: 1656654 - sodium bicarbonate 1020 MG Granules for Oral Solution
  • RxCUI: 1656654 - NaHCO3 1020 MG Granules for Oral Solution
  • RxCUI: 1656660 - Brioschi 1.02 GM Granule for Oral Solution
  • RxCUI: 1656660 - sodium bicarbonate 1020 MG Granules for Oral Solution [Brioschi Antacid]

* Please review the full disclaimer at the bottom of this page.

Patient Education

Sodium Bicarbonate


Sodium bicarbonate is an antacid used to relieve heartburn and acid indigestion. Your doctor also may prescribe sodium bicarbonate to make your blood or urine less acidic in certain conditions. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
[Learn More]


* Please review the full disclaimer at the bottom of this page.

Product & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the FDA Application Number? This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the End Marketing Date? This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".