SODIUM BICARBONATE description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

SODIUM BICARBONATE

Mirror Pharmaceuticals LLC
Mirror Pharmaceuticals LLC

SODIUM BICARBONATE 10 gr (650 mg)


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

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

Warnings

Do not use this product if you are on a sodium-restricted diet unless directed by a doctor. Do not take more than 24 tablets for adults up to 60 years of age (or 12 tablets for adults 60 years of age and older) in a 24-hour period nor use the maximum dosage for more than 2 weeks, except under the advice and supervision of a physician.

As with any drug, if you are pregnant or nursing a baby, seek advise of a health professional before using this product.

STOMACH WARNING:

TO AVOID SERIOUS INJURY, DO NOT TAKE UNTIL TABLET IS COMPLETELY DISSOLVED. IT IS VERY IMPORTANT NOT TO TAKE THIS PRODUCT WHEN OVERLY FULL FROM FOOD OR DRINK. Consult a doctor if severe stomach pain occurs after taking this product.

DRUG INTERACTION PRECAUTION:

Antacids may interact with certain prescription drugs. If you are presently taking a prescription drug, do not take this product without checking with your physician or other health professional.

Directions:

  • Adults - Take 1 tablet, dissolved in a glass of water, as needed.
  • Maximum daily dose for adults upto 60 years of age is 24 tablets.
  • Maximum daily dose for adults 60 years of age and older is 12 tablets.
  • Dissolve completely in water before drinking.
  • DO NOT EXCEED RECOMMENDED DOSE. Not recommended for children.

Other Information:

  • each tablet contains: sodium 178 mg (7.74 meq)
  • store at room temperature 15°- 30°C (59°- 86°F) in well-closed containers as defined in the USP.

Inactive Ingredients:

Pregelatinized starch, NF and mieral oil, USP.

KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN.

In case of accidental overdose, seek professional assistance or contact a poison control center immediately.

SODIUM BICARBONATE

SODIUM BICARBONATE

SODIUM BICARBONATE TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52682-206
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM BICARBONATE 650 mg

Inactive Ingredients

Ingredient Name Strength
Mineral Oil
STARCH, CORN

Product Characteristics

Color Size Imprint Code Shape
WHITE (White) 11 mm CL;206 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52682-206-04 1000 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2011-01-24


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.