0135-0574 : Gaviscon Oral Liquid


NDC: 0135-0574
Labeler: Glaxosmithkline Consumer Healthcare Lp
Product Type: Human OTC Drug
Drug Name:  Gaviscon
Dosage Form: Oral Liquid
Application #: part331
Rev. Date: 


NDC Package Codes:

  • 0135-0574-01: 355 ML IN 1 BOTTLE (0135‑0574‑01)

Active Ingredients:

  • Aluminum Hydroxide
  • Magnesium Carbonate

Dosage Strength:

  • 254 mg/5mL
  • 237.5 mg/5mL

Related Products:

Based on records with the same trade name.
  • 0135-0094 Gaviscon Oral Liquid by Glaxosmithkline Consumer Healthcare Lp
  • 0135-0095 Gaviscon Oral Liquid by Glaxosmithkline Consumer Healthcare Lp
  • 0135-0096 Gaviscon Chewable 80/14.2 Chewable Tablet by Glaxosmithkline Consumer Healthcare Lp
  • 0135-0098 Gaviscon Extra Strength (Aluminum Hydroxide 160 mg / Magnesium Carbonate 105 mg) Chewable Tablet by Glaxosmithkline Consumer Healthcare Lp
  • 0135-0430 Gaviscon Extra Strength (Aluminum Hydroxide 160 mg / Magnesium Carbonate 105 mg) Chewable Tablet by Glaxosmithkline Consumer Healthcare Lp

NDC QR Code

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NDC 0135-0574 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.