FDA Label for Plus Pharma Calcium Antacid

View Indications, Usage & Precautions

Plus Pharma Calcium Antacid Product Label

The following document was submitted to the FDA by the labeler of this product A-s Medication Solutions. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Active Ingredient (In Each Tablet)



Calcium Carbonate, USP 500 mg



Purpose



Antacid



Uses



for the relief of



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

Warnings



Do not take more than 15 tablets in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.



Ask A Doctor Or Pharmacist Before Use If You Are



  • presently taking a prescription drug. Antacids may interact with certain prescription drugs.

If Pregnant Or Breast-Feeding,



ask a doctor before use.



Directions



Adults and children 12 years and older

  • Chew 2 tablets every 2 or 3 hours as symptoms occur or as directed by a doctor
  • Children under 12 years

    • Do not give to children under 12 years unless directed by a doctor

Other Information



  • Each tablet contains: Elemental Calcium 195 mg
  • Each tablet contains: Sugar 1g
  • Do not exceed recommended dosage
  • Store at room temperature in a dry place
  • Do not use if clear neck seal is broken or missing

Inactive Ingredients



Acacia, Artificial Cherry Flavor, Artificial Red Berry Flavor, Colloidal Silica, D and C Red #27 Lake, FD and C Blue #1 Lake, Magnesium Stearate, Maltodextrin, Microcrystalline Cellulose, Natural and Artificial Spearmint Flavor, Strach, Sucrose



Questions?



If you have any questions or comments, or to report an adverse event, please contact (800) 795-9775.



How Supplied



Product: 50090-4478

NDC: 50090-4478-0 150 TABLET, CHEWABLE in a BOTTLE, PLASTIC


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