Ultra Strength Gas Relief
Product Images NDC 51013-123

3 FDA label images from Puracap Pharmaceutical Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ultra Strength Gas Relief (NDC 51013-123). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Puracap Pharmaceutical Llc, 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

Ddm08-03 Back (Ddm08 03 Back)

Ddm08-03 Back (Ddm08 03 Back)
Drug Facts label for Ultra Strength Gas Relief softgels with active ingredient Simethicone 180 mg listed as an anti-gas agent. The label includes uses, warnings, directions, storage instructions, inactive ingredients, contact information, and a satisfaction guarantee statement for the PuraCap Pharmaceutical LLC product.*
FDA Label Image

Ddm08-03 Front (Ddm08 03 Front)

Ddm08-03 Front (Ddm08 03 Front)
The packaging label for Ultra Strength Gas Relief softgels from Discount Drug Mart Food Fair shows the proprietary name Ultra Strength Gas Relief with active ingredient Anti-Gas/Simethicone 180 mg. It highlights 60 easy to swallow softgels per package and mentions relief for pressure, bloating, and gas distress. The label also includes anti-theft device text and a comparison to the active ingredient in Phazyme Ultra Strength.*
FDA Label Image

Ddm09-03 (Ddm09 03)

Ddm09-03 (Ddm09 03)
Ultra Strength Gas Relief softgels label with active ingredient Simethicone 180 mg each. The label indicates 60 softgels per package and highlights anti-gas purpose, ease of swallowing, and dosage warnings. It displays branding for Drug Mart and PuraCap Pharmaceutical LLC as the distributor.*

* 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.