Humco Sodium Bicarbonate

SODIUM BICARBONATE ORAL HUMAN OTC DRUG

Humco Sodium Bicarbonate is an FDA drug label for the active ingredient SODIUM BICARBONATE manufactured by Humco Holding Group, Inc. 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 20260526.

Generic name
SODIUM BICARBONATE
Manufacturer
Humco Holding Group, Inc.
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
0395-2685
Application
M001
Label effective
20260526

About this product

Humco Sodium Bicarbonate is an FDA-registered drug product whose active ingredient is SODIUM BICARBONATE. It is labelled by Humco Holding Group, Inc. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 0395-2685, application M001, label effective 20260526. It is one of 33 FDA drug label records sharing the active ingredient SODIUM BICARBONATE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing SODIUM BICARBONATE are most often described in connection with: relief heartburn, acid indigestion, upset stomach. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Soduim Bicarbonate, USP

Indications & Usage

Use For relief of heartburn, acid indigestion, and upset stomach associated with these symptoms.

Dosage & Administration

Directions Adult and children 12 yrs of age and older: Dissolve 1/2 level teaspoon in glass (4 fl oz) of water every 2 hours up to maximum dosafe or as directed by doctor. Dissolve completely in water before drinking. Do not exceed recommended dose. SEE WARNINGS.

Warnings

Warnings FOR ORAL USE ONLY Except under supervision of a doctor: Do not administer to children under 12 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. STOMACH WARNING: TO AVOID SERIOUS INJURY, DO NOT TAKE UNTIL POWDER IS COMPLETELY DISSOLVED. IT IS VERY IMPORTANT NOT TO TAKE THIS PRODUCT WHEN OVERLY FULL FROM FOOD OR DRINK. FOR ORAL USE ONLY Except under supervision of a doctor: Do not administer to children under 12 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. STOMACH WARNING: TO AVOID SERIOUS INJURY, DO NOT TAKE UNTIL POWDER IS COMPLETELY DISSOLVED. IT IS VERY IMPORTANT NOT TO TAKE THIS PRODUCT WHEN OVERLY FULL FROM FOOD OR DRINK.

More products with the same ingredient

SODIUM BICARBONATE

Arm and Hammer Baking Soda

Church & Dwight Co., Inc. View label

Medis Sodium Bicarbonate

Humco Holding Group, Inc View label

SODIUM BICARBONATE

Medical Purchasing Solutions, LLC View label

SODIUM BICARBONATE

Richmond Pharmaceuticals, Inc. View label

SODIUM BICARBONATE

HF Acquisition Co LLC, DBA HealthFirst View label

SODIUM BICARBONATE

HF Acquisition Co LLC, DBA HealthFirst View label

SODIUM BICARBONATE

Medical Purchasing Solutions, LLC. View label

How products containing SODIUM BICARBONATE compare

FDA lists 33 drug label records with SODIUM BICARBONATE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — Medical Purchasing Solutions, LLC 5
— — Exela Pharma Sciences, LLC 3
— — A-S Medication Solutions 2
— — HF Acquisition Co LLC, DBA HealthFirst 2
— — Richmond Pharmaceuticals, Inc. 2

Frequently asked questions

What is Humco Sodium Bicarbonate used for?
Use For relief of heartburn, acid indigestion, and upset stomach associated with these symptoms.

Who makes Humco Sodium Bicarbonate?
Humco Holding Group, Inc. is the labeler of record for Humco Sodium Bicarbonate. 33 FDA label records share the active ingredient SODIUM BICARBONATE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Humco Sodium Bicarbonate come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Humco Sodium Bicarbonate prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing SODIUM BICARBONATE?
Yes. 33 FDA drug label records list SODIUM BICARBONATE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Humco Sodium Bicarbonate been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.