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  4. NDC Product Code: 53807-137 Riginic Antacid Liquid

NDC 53807-137 Riginic Antacid Liquid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 53807-137?
  5. Riginic Antacid Liquid Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
53807-137
Proprietary Name:
Riginic Antacid Liquid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rij Pharmaceutical Corporation
Labeler Code:
53807
Product Label ID:
be7fb10d-dda0-41ae-8122-2ff74180ae92
Start Marketing Date: [9]
04-03-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Flavor(s):
MINT (C73404 - COOL MINT)

Code Structure Chart

Product Details

What is NDC 53807-137?

The NDC code 53807-137 is assigned by the FDA to the product Riginic Antacid Liquid which is product labeled by Rij Pharmaceutical Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53807-137-12 355 ml 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 Riginic Antacid Liquid?

•shake well before using•do not take more than 8 tablespoons in 24 hours•do not use the maximum dosage for more than 2 weeks•dosage: 1-2 tablespoons after meals and at bedtime followed by milk or water

Which are Riginic Antacid Liquid UNII Codes?

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

Which are Riginic Antacid Liquid 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 Riginic Antacid Liquid?

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: 252203 - aluminum hydroxide 95 MG / magnesium carbonate 358 MG in 15 mL Oral Suspension
  • RxCUI: 252203 - aluminum hydroxide 6.33 MG/ML / magnesium carbonate 23.9 MG/ML Oral Suspension
  • RxCUI: 252203 - aluminum hydroxide 31.7 MG / magnesium carbonate 119.3 MG per 5 ML Oral Suspension
  • RxCUI: 252203 - aluminum hydroxide 32 MG / magnesium carbonate 119 MG per 5 ML Oral Suspension
  • RxCUI: 252203 - aluminum hydroxide 95 MG / magnesium carbonate 358 MG per 15 ML Oral Suspension

* 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".