Nexmed Multi Symptom Stomach Relief Capsule, Liquid Filled
Product Images NDC 83059-0092

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Nexmed Multi Symptom Stomach Relief (NDC 83059-0092). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Shield Pharmaceuticals Corp, 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

Stomach Relief Label 105 Back (Stomach Relief Label 105 Back)

Stomach Relief Label 105 Back (Stomach Relief Label 105 Back)
Drug Facts panel for nexmed multi symptom stomach relief capsule with bismuth subsalicylate 262 mg. The panel includes warnings about use in children, allergy alerts, instructions to ask a doctor or pharmacist before use if certain conditions exist, directions for adults and children over 12 years, and other information including storage conditions and inactive ingredients. A 'Did you know?' section explains bismuth subsalicylate's use in treating digestive discomfort and notes that it may cause tongue and stool to turn black temporarily.*
FDA Label Image

Stomach Relief Label 105 Front (Stomach Relief Label 105 Front)

Stomach Relief Label 105 Front (Stomach Relief Label 105 Front)
Label for nexmed multi-symptom stomach relief softgels containing Bismuth subsalicylate 262 mg. The product is indicated as an upset stomach reliever and anti-diarrheal with 105 softgel capsules in the package. Distributed by nexmed, Holbrook, NY, and labeled as FSA/HSA eligible. The label highlights relief for five symptoms: nausea, diarrhea, heartburn, indigestion, and upset stomach. Includes a barcode and tamper-evident seal warning.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.