Ultra Bismuth Liquid
Product Images NDC 55910-637

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Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Ultra Bismuth (NDC 55910-637). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dolgencorp, Inc. (dollar General & Rexall), these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Bismuth Subsalicylate 525 mg (Peptic Relief Ultra Strength No Veegum Liquid 1)

Bismuth Subsalicylate 525 mg (Peptic Relief Ultra Strength No Veegum Liquid 1)
This is a drug information and warnings section for a product that relieves diarrhea, traveler's diarrhea, overindulgence in food and drink, upset stomach, heartburn, indigestion, and nausea. It is recommended to not take more than 8 doses (120 mL) in 24 hours and not use any other dosing device. It should be kept out of reach of children and should not be used by pregnant or breastfeeding women without consultation with a health professional. In case of overdose, medical help or Poison Control Center should be contacted. Each 15 ml contains 206mg low sodium and it should be protected from freezing and excessive heat (over 104°F or 40°C). Ingredients include sodium 5 mg, venzoic acid, DG red #22, DAC red #28, flavor, glycerin, purified water, sucrose, and xanthan gum. No brand name or actual drug name is mentioned.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.