NDC 69276-200 Brioschi Effervescent Antacid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69276 - Neobourne Pharma Lp
- 69276-200 - Brioschi Effervescent Antacid
Product Characteristics
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?
What are the uses for Brioschi Effervescent Antacid?
Which are Brioschi Effervescent Antacid UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
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:
- SUCROSE (UNII: C151H8M554)
- LEMON (UNII: 24RS0A988O)
- MALIC ACID (UNII: 817L1N4CKP)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- CORN SYRUP (UNII: 9G5L16BK6N)
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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.
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[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".