Bio-sorb
Product Images NDC 51021-302

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Bio-sorb (NDC 51021-302). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sircle Laboratories, 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

Chemical Structure (Diclofenac 01)

Chemical structure of Diclosaicin showing a sodium carboxylate group attached to a benzene ring with two chloro substituents on a connected aromatic ring and an amine linkage.*

FDA Label Image

Figure A (Diclofenac 02)

An instructional illustration labeled 'Figure A' showing two methods of applying a topical product by hand. The left side depicts a hand forming a circle with the thumb and index finger while the other hand is open below it, and the right side shows a similar hand position on the inner forearm. The image is related to the application technique for Diclosaicin by Chadwick Pharmaceuticals, Inc.*

FDA Label Image

Figure B (Diclofenac 03)

Illustration showing a person applying a topical product, with hand movements directed around the shoulder and upper arm area, as indicated by arrows. This figure likely demonstrates the application technique for Diclosaicin topical use.*

FDA Label Image

Figure C (Diclofenac 04)

An instructional line drawing labeled 'Figure C' depicts a hand demonstrating the application of a topical product on the knee area with a circular motion, indicating usage directions likely related to Diclosaicin by Chadwick Pharmaceuticals, Inc.*

FDA Label Image

Principal Display Panel (Kit Carton Label)

Label for Diclosaicin, a prescription product by Chadwick Pharmaceuticals, Inc, including diclofenac sodium topical solution 1.5% w/w (5 fl oz/150 ml) and capsaicin cream 0.025% (8 fl oz/237 ml). The label displays NDC 70981-0702-01 and specifies kit contents with corresponding active ingredient strengths.*

* 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.