Active Ingredient (In Each Fast Gel)
Simethicone 500mg
Phazyme Ultimate Capsule, Liquid Filled
FDA Label NDC 0132-0222
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by C.b. Fleet Company, Inc. for the product Phazyme Ultimate (NDC 0132-0222). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each fast gel), purpose, use, stop use and ask a doctor if, directions, other information, inactive ingredients, questions?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Anti-gas
Use
- Relieves bloating, pressure, or fullness commonly referred to as gas.
Stop Use And Ask A Doctor If
condition persists.
Directions
- Swallow (1) Fast Gel as symptoms occur
- Do not exceed (1) Fast Gel per 24 hours except under the advice and supervision of a physician
Other Information
- Store at room temperature 59°- 86°F (15°-30°C).
Inactive Ingredients
FD&C blue no. 1, gelatin, glycerin, medium-chain triglycerides, silicon dioxide, sorbitol, water
Questions?
Call toll-free 1-855-727-4277
Principal Display Panel
PHAZYME®
ANTI-GAS SIMETHICONE 500mg
ULTIMATE
500 MG
A Purple Box With White Textdescription Automatically Generated (Phazyme Ultimate 500 mg 0132 0222 01)
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