Diclofenac Potassium Capsule, Liquid Filled
Product Images NDC 59088-131

View Photos of 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 Diclofenac Potassium (NDC 59088-131). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Puretek Corporation, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Label (Container Label)

Label (Container Label)
Label for Diclofenac Potassium Capsules 25 mg by PureTek Corporation. The label indicates 120 liquid-filled capsules with directions for adult dosage, storage conditions, and manufacturing information. The product is distributed by PureTek Corporation in Panorama City, CA, and manufactured by Strides Pharma Science Ltd., India. Includes a barcode and Rx only designation.*
FDA Label Image

Figure 1 (Figure 1)

Figure 1 (Figure 1)
Line graph titled 'Mean Pain Intensity Scores at the Midpoint and End of Each Dose Interval in Postbunionectomy Pain Study 1' showing mean pain intensity over time across nine dosing intervals for Diclofenac Potassium 25 mg (Zipzor) versus placebo, with pain intensity on the y-axis (0=no pain to 10=worst pain) and dose intervals on the x-axis. The graph plots two lines representing 25 mg Zipzor (triangle markers) and placebo (circle markers), illustrating pain reduction trends over 48 hours.*
FDA Label Image

Chemical Structure (Structure)

Chemical Structure (Structure)
Chemical structure diagram of Diclofenac Potassium, showing two aromatic rings, chlorine atoms, and a potassium carboxylate group.*

* 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.