50090-1538 : Mintox Oral Suspension


NDC: 50090-1538
Labeler: A-s Medication Solutions
Product Type: Human OTC Drug
Drug Name: Mintox
Dosage Form: Oral Suspension
Application #: part331
Rev. Date: 


NDC Package Codes:

  • 50090-1538-0: 355 ML IN 1 BOTTLE (50090‑1538‑0)

Active Ingredients:

  • Aluminum Hydroxide
  • Magnesium Hydroxide
  • Dimethicone

Dosage Strength:

  • 200 mg/5mL
  • 200 mg/5mL
  • 20 mg/5mL

Pharmaceutical Classes:

  • Calculi Dissolution Agent [EPC]
  • Increased Large Intestinal Motility [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]
  • Magnesium Ion Exchange Activity [MoA]
  • Osmotic Activity [MoA]
  • Osmotic Laxative [EPC]
  • Skin Barrier Activity [PE]
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Related Products:

Based on records with the same trade name.
  • 0904-5721 Mintox Oral Suspension by Major Pharmaceuticals Inc.
  • 0904-6764 Mintox Oral Suspension by Major Pharmaceuticals
  • 17856-5721 Mintox Oral Suspension by Atlantic Biologicals Corps
  • 17856-6764 Mintox Oral Suspension by Atlantic Biologicals Corp.

NDC QR Code

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NDC 50090-1538 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.