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Sodium Bicarbonate by Rugby Laboratories, Inc.

Dosage form: tablet
Ingredients: Sodium Bicarbonate 650mg
Labeler: Rugby Laboratories, Inc.
NDC Code: 0536-4544

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts for Sodium Bicarbonate 650 mg

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Active ingredient                                           Purpose

(in each tablet)

Sodium bicarbonate 10 gr (650 mg) .......      Antacid

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Purpose                      Antacid

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Keep out of reach of children.

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Uses relieves

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

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Ask a doctor before use if you have a sodium restricted diet

Ask a doctor or pharmacist before use of you are

taking a prescription drug. Antacids may interact with

certain prescription drugs.

Stop use and ask a doctor if symptoms last more than 2 weeks

If pregnant or breast-feeding, ask a health professional before use.

Each tablet contains: sodium 178 mg

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  • adults 60 years of age and over: 1-2 tablets every 4 hours, not more than 12 tablets in 24 hours
  • adults under 60 years of age: 1-4 tablets every 4 hours, not more than 24 tablets in 24 hours
  • do not use the maximum dosage for more than 2 weeks
  • tablets may be swallowed whole or dissolved in water prior to use

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Inactive ingredients

croscarmellose sodium, microcrystalline cellulose, stearic acid

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store at room temperature 15o - 30o C (59o - 86o F)

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Questions or comments?

call 1-800-645-2158, 9 am - 5 pm ET,  Monday - Friday

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sodium bicarbonate tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0536-4544
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sodium Bicarbonate (Sodium Cation) Sodium Bicarbonate650 mg
Inactive Ingredients
Ingredient NameStrength
Product Characteristics
ColorwhiteScoreno score
ShapeROUND (Tablet) Size11mm
FlavorImprint Code119
#Item CodePackage Description
1NDC:0536-4544-101000 TABLET (TABLET) in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33103/08/2010
Labeler - Rugby Laboratories, Inc. (109178264)
Registrant - Advance Pharmaceutical, Inc. (187824339)
Advance Pharmaceutical, Inc.187824339manufacture, repack, relabel

Revised: 12/2010
Rugby Laboratories, Inc.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.