Diclofenac Sodium Solution
Product Images NDC 65162-911

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 65162-911). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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

Muscle Rub (Muscle Rub Tube)

Muscle Rub (Muscle Rub Tube)
This is a CareALL Muscle Rub greaseless pain relieving cream label. The net weight is 3 ounces (85 grams). The label includes drug facts listing menthol 10% and methyl salicylate 15% as active ingredients, both serving as topical analgesics. The product is distributed by CareALL Products in Nashville, Tennessee.*
FDA Label Image

Orthrexo Packaging (Orthrexo Carton)

Orthrexo Packaging (Orthrexo Carton)
Orthrexo kit packaging label for a prescription drug by V2 Pharma, LLC. It contains Diclofenac Sodium Topical Solution 1.5% (150 mL) and Muscle Rub Pain Relieving Cream 3 oz. (85 grams). The design features a blue and white color scheme with purple highlights, product name, NDC 72835-333-02, and storage instructions on the carton.*
FDA Label Image

Structural Formula (Diclofenac Sodium Topical Solution 1)

Structural Formula (Diclofenac Sodium Topical Solution 1)
Chemical structure of diclofenac sodium, showing the molecular arrangement including two chlorine atoms, an amine group, and a carboxylate sodium salt.*
FDA Label Image

Figure A1 (Diclofenac Sodium Topical Solution 2)

Figure A1 (Diclofenac Sodium Topical Solution 2)
An instructional line drawing showing a person dispensing liquid from a bottle onto the palm of their opposite hand. The image appears to demonstrate the proper method for applying a liquid medication or topical solution.*
FDA Label Image

Figure A2 (Diclofenac Sodium Topical Solution 3)

Figure A2 (Diclofenac Sodium Topical Solution 3)
Illustration showing a hand applying a topical product to the inner forearm of the opposite arm. The image demonstrates correct application technique likely related to the use of Orthrexo topical kit containing Diclofenac Sodium, Menthol, and Methyl salicylate.*
FDA Label Image

Figure B (Diclofenac Sodium Topical Solution 4)

Figure B (Diclofenac Sodium Topical Solution 4)
An instructional line drawing showing how to apply a topical product to the knee. The illustration depicts a hand applying the medication with arrows indicating downward motion on the front and side of the knee area.*
FDA Label Image

Figure C (Diclofenac Sodium Topical Solution 5)

Figure C (Diclofenac Sodium Topical Solution 5)
An instructional illustration showing a hand grasping a knee with an arrow indicating a circular motion around the knee. This diagram likely demonstrates the application or massage technique for a topical product.*
FDA Label Image

Label (Diclofenac Sodium Topical Solution 6)

Label (Diclofenac Sodium Topical Solution 6)
Label for Diclofenac Sodium Topical Solution, 1.5% w/w, a prescription drug in a 5 fl oz (150 mL) bottle. Includes dosage instructions of 40 drops to a knee, four times a day, warnings to avoid contact with eyes and mucous membranes, and storage conditions. Distributed by Amneal Pharmaceuticals, Bridgewater, NJ. Contains excipients such as alcohol and glycerin.*
FDA Label Image

Carton (Diclofenac Sodium Topical Solution 7)

Carton (Diclofenac Sodium Topical Solution 7)
This image shows a flat packaging label for Diclofenac Sodium Topical Solution, 1.5% w/w by Amneal Pharmaceuticals. The label includes product warnings, usage instructions, net contents of 5 fl oz (150 mL), a barcode, and the NDC number 65162-911-74. It states the product is for external use only and prescription use (Rx only).*

* 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.