Sutab Tablet
Product Images NDC 24338-201

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Sutab (NDC 24338-201). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Azurity Pharmaceuticals, Inc., 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

Pot Chlo (Kcl)

Pot Chlo (Kcl)
An illustration showing a dashed line connecting the chemical symbols 'Cl⁻' (chloride ion) on the left and 'K⁺' (potassium ion) on the right, likely representing an ionic interaction or relation between chloride and potassium ions.*
FDA Label Image

Mg Sulf (Mgso4)

Mg Sulf (Mgso4)
Chemical structure diagram showing the sulfate ion complexed with a magnesium ion (Mg2+). The image depicts one sulfur atom centrally bonded to four oxygen atoms in a tetrahedral arrangement, with magnesium indicated as a 2+ charged cation.*
FDA Label Image

Sod Sulf (Na2so4)

Sod Sulf (Na2so4)
Chemical structure diagram of sodium sulfate showing sulfate ion with two sodium ions.*
FDA Label Image

Sutab Carton (Sutab Carton)

Sutab Carton (Sutab Carton)
Label for SUTAB tablets containing sodium sulfate, magnesium sulfate, and potassium chloride. Each carton contains two 12-tablet bottles, for a total of 24 tablets. The label includes dosing guidelines for colonoscopy preparation, noting the need to remove and discard desiccants. Manufactured by Azurity Pharmaceuticals, Inc., the label shows the NDC 24338-201-01, with instructions and dietary guidelines for usage.*
FDA Label Image

Sutab Label (Sutab Label)

Sutab Label (Sutab Label)
Label for SUTAB tablets containing sodium sulfate, magnesium sulfate, and potassium chloride. Displays active ingredient strengths as 1.479 g, 0.225 g, and 0.188 g respectively. Label includes storage instructions, a warning to remove and discard desiccant, and the NDC 24338-202-01. Manufactured by Azurity Pharmaceuticals, Inc.*

* 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.