NDC 69276-200 Brioschi Effervescent Antacid

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:
69276-200
Proprietary Name:
Brioschi Effervescent Antacid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Neobourne Pharma Lp
Labeler Code:
69276
Start Marketing Date: [9]
11-27-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

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

Product Packages

NDC Code 69276-200-05

Package Description: 10 PACKET in 1 CARTON / 5 g in 1 PACKET

NDC Code 69276-200-58

Package Description: 300 g in 1 BOTTLE

Product Details

What is NDC 69276-200?

The NDC code 69276-200 is assigned by the FDA to the product Brioschi Effervescent Antacid which is product labeled by Neobourne Pharma Lp. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69276-200-05 10 packet in 1 carton / 5 g in 1 packet, 69276-200-58 300 g in 1 bottle . 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 Brioschi Effervescent Antacid?

• Fully dissolve 5 g (1 teaspoon) in 4-6 ounces of water before drinking • Do not use more than directedAdults and children 12 years and older One (1 teaspoon) dose each hour Do not exceed 8 doses in 24 hours Adults 60 years and older One (1 teaspoon) dose each hour Do not exceed 4 doses in 24 hoursChildren under 12Ask a doctor

Which are Brioschi Effervescent Antacid UNII Codes?

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

Which are Brioschi Effervescent Antacid 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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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]


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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".