NDC 70242-131 Sodium Bicarbonate 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:
70242-131
Proprietary Name:
Sodium Bicarbonate Antacid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dannso Corp./d.b.a. Essential Products
Labeler Code:
70242
Start Marketing Date: [9]
09-25-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 70242-131-04

Package Description: 113 g in 1 BOTTLE, PLASTIC

Product Details

What is NDC 70242-131?

The NDC code 70242-131 is assigned by the FDA to the product Sodium Bicarbonate Antacid which is product labeled by Dannso Corp./d.b.a. Essential Products. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70242-131-04 113 g in 1 bottle, plastic . 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 Sodium Bicarbonate Antacid?

Take ½ level teaspoon in ½ glass (4 fl. oz.) of water every 2 hours up to maximum dosage or as directed by a doctor. Dissolve completely in water before drinking.AgeMaximum DosageAdults 60 years and overDo not exceed three doses of 1/2 teaspoon in a 24 hour period.Adults and children 12 years and overDo not exceed six doses of 1/2 teaspoon in a 24 hour period.Children under 12 yearsDo not use.Do not exceed recommended dosage. See warnings.

Which are Sodium Bicarbonate Antacid UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Sodium Bicarbonate Antacid?

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:

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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".