Sodium Bicarbonate
Sodium Bicarbonate is an FDA drug label for the active ingredient SODIUM BICARBONATE manufactured by Pharma Nobis, LLC administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231222.
- Generic name
- SODIUM BICARBONATE
- Manufacturer
- Pharma Nobis, LLC
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 82645-904
- Application
- M001
- Label effective
- 20231222
Active ingredients
Indications & Usage
Use For relief of heartburn, acid indigestion, and upset stomach associated with these symptoms.
Dosage & Administration
Directions Adult and children 6 yrs of age and older: Take 1/2 tsp. in 1/2 g;ass (4 fl oz) of water every 2 hrs. up to maximum dosage or as directed by doctor.
Contraindications
Not available.
Warnings
Warnings NOT FOR INJECTIONS Except under supervision of a doctor do not administer to children under 6 years of age. Do not take more than six, 1/2 tsp. per person up to 60 years old, or three 1/2 tsp. per person 60 years or older in a 24 hour period. Do not use this product if you are on a sodium restricted diet (each 1/2 tsp. contains 30 mEq (0.7 g) Sodium). Do not use the maximum does more than 2 weeks.
Adverse Reactions
Not available.