Diclofenac Potassium Capsule, Liquid Filled
Product Images NDC 69315-275

3 FDA label images from Leading Pharma, 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 Diclofenac Potassium (NDC 69315-275). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Leading Pharma, 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

Chemstructure (Chemstructure)

Chemstructure (Chemstructure)
Chemical structure of Diclofenac Potassium, illustrating the molecular arrangement including two chlorinated benzene rings, an amine group, a carboxylate group, and a potassium ion.*
FDA Label Image

Containerlabel (Containerlabel)

Containerlabel (Containerlabel)
Label for Diclofenac Potassium 25 mg liquid filled capsules, containing 120 capsules per bottle. The label shows the NDC number 69315-275-20, the product name and strength prominently, and indicates it is Rx only. The labeler is Leading Pharma, LLC, located in Fairfield, NJ, USA. Storage instructions and product origin (Taiwan) are also included.*
FDA Label Image

Figure01 (Fig01)

Figure01 (Fig01)
A line graph comparing mean pain intensity over 48 hours between a 25 mg Diclofenac Potassium group and a placebo group with QID dosing intervals. The y-axis shows pain intensity on a scale from 0 (no pain) to 10 (worst pain), and the x-axis marks variable time points including the end of each dosing day from Day 1 to Day 9. Two lines represent the 25 mg Diclofenac Potassium (marked with triangles) and placebo (marked with circles) groups.*

* 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.