Sodium Bicarbonate Tablet
FDA Label NDC 54738-020

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Richmond Pharmaceuticals, Inc. for the product Sodium Bicarbonate (NDC 54738-020). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding drug facts, purpose, indications:, ask a doctor or pharmacist, directions:, other information:, inactive ingredient, questions or comments, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient (in each tablet)

Sodium bicarbonate 10 gr (650 mg)

Purpose

Antacid

Indications:

Relieves:

  • acid indigestion
  • heartburn
  • sour stomach
  • upset stomach associated with these symptoms

Ask A Doctor Or Pharmacist

  • if you are on a sodium-restricted diet.
  • if you are taking a prescription drug. Antacids may interact with certain prescription drugs.
  • if symptons last more than 2 weeks

Directions:

  • Adults 60years of age and over - 1-2 tablets every 4 hours. Not more than 12 tablets in 24 hours
  • Adults under 60 years- 1-4 tablets every4 hours. Not more than 24 tablets in 24 hours
  • Dissolve tabelt completely in water before drinking.
  • DO NOT EXCEED RECOMMENDED DOSE. Not recommended for children.

Other Information:

  • each tablet contains: sodium 178 mg 
  • store at room temperature 15 °- 30 °C (59 °- 86 °F).

Inactive Ingredient

croscarmellose sodium, microcrystalline cellulose, stearic acid

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