Magnesium Oxide Tablet
FDA Label NDC 50090-7432

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by A-s Medication Solutions for the product Magnesium Oxide (NDC 50090-7432). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding other, active ingredient, purpose, use, ask a doctor before use if, otc - do not use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

Active Ingredient

Magnesium Oxide 400 mg (241.3 mg Elemental Magnesium)

Purpose

Antacid

Use

relieves:

  • acid indigestion
  • upset stomach

Ask A Doctor Before Use If

  • you have kidney disease
  • you are taking a prescription drug (antacids may interact with certain prescription drugs)
  • you are pregnant or breast feeding.

Otc - Do Not Use

Do not take more than 2 tablets in a 24 hour period.

  • May have a laxative effect.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Directions

  • take one or two antacid tablets daily. Do not exceed two tablets unless directed by a physician.

Other Information

  • Store at controlled room temperature 15° to 30°C (59° to 86°F).
  • Tamper evident, do not use if imprinted safety seal under cap is broken or missing.

Inactive Ingredients

Corn Starch, Croscarmellose Sodium, Magnesium Stearate, Microcrystalline Cellulose, Silicon Dioxide, Stearic Acid.

Questions?

Call 1-844-221-7294 M-F 9am - 5pm EST

How Supplied

Product: 50090-7432

NDC: 50090-7432-0 120 TABLET in a BOTTLE

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