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  4. NDC Product Code: 10237-591 Arm And Hammer Baking Soda

NDC 10237-591 Arm And Hammer Baking Soda

Sodium Bicarbonate Powder, For Solution Oral - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 10237-591?
  5. Arm And Hammer Baking Soda Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
10237-591
Proprietary Name:
Arm And Hammer Baking Soda
Non-Proprietary Name: [1]
Sodium Bicarbonate
Substance Name: [2]
Sodium Bicarbonate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Powder, For Solution - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a solution.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Church & Dwight Co., Inc.
    Labeler Code:
    10237
    Product Label ID:
    643fe204-4a7b-00e4-e053-2a91aa0aef06
    FDA Application Number: [6]
    M016
    Marketing Category: [8]
    OTC MONOGRAPH DRUG -
    Start Marketing Date: [9]
    01-01-2000
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Characteristics

    Imprint(s):
    WHITE

    Code Structure Chart

    Product Details

    What is NDC 10237-591?

    The NDC code 10237-591 is assigned by the FDA to the product Arm And Hammer Baking Soda which is a human over the counter drug product labeled by Church & Dwight Co., Inc.. The generic name of Arm And Hammer Baking Soda is sodium bicarbonate. The product's dosage form is powder, for solution and is administered via oral form. The product is distributed in 8 packages with assigned NDC codes 10237-591-01 454 g in 1 carton , 10237-591-02 907 g in 1 carton , 10237-591-04 1810 g in 1 carton , 10237-591-08 227 g in 1 carton , 10237-591-12 5443 g in 1 bag , 10237-591-14 6804 g in 1 bag , 10237-591-20 6123 g in 1 bag , 10237-591-35 1588 g in 1 carton . 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 Arm And Hammer Baking Soda?

    • add 1/2 teaspoon to 1/2 glass (4 fl. oz.) of water every 2 hours, or as directed by physician. Dissolve completely in water. Accurately measure 1/2 teaspoon.• do not take more than the following amounts in 24 hours: • seven 1/2 teaspoons • three 1/2 teaspoons if your are over 60 years• do not sue the maximum dosage for more than 2 weeksOther information:• each 1/2 teaspoon contains 616mg sodium.

    What are Arm And Hammer Baking Soda Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
    • SODIUM BICARBONATE 1 g/g - A white, crystalline powder that is commonly used as a pH buffering agent, an electrolyte replenisher, systemic alkalizer and in topical cleansing solutions.

    Which are Arm And Hammer Baking Soda UNII Codes?

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

    Which are the Pharmacologic Classes for Arm And Hammer Baking Soda?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [6] 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.

    [8] 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.

    [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".