Muscle Rub
Product Images NDC 45802-174

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Muscle Rub (NDC 45802-174). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Padagis Israel Pharmaceuticals Ltd, 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

Bottle (Bottle)

Label for Diclofenac Sodium 1.5% w/w topical solution, 150 mL, labeled by Apotex Corp. The label includes dosage instructions, warning, active ingredient concentration (16.05 mg diclofenac sodium per mL), excipients list, storage information, and manufacturer details for Apotex Inc. in Toronto, Ontario, Canada, and Apotex Corp. in Weston, Florida. The label also displays the NDC code 60505-0399-5 and a barcode.*

FDA Label Image

Carton (Carton)

Label for Diclofenac Sodium 1.5% w/w topical solution, 150 mL, by Apotex Corp. The label includes dosage instructions, warnings, and ingredients. It states the product is for external use only and prescription use (Rx only). Storage instructions and manufacturer information for Apotex Inc. and Apotex Corp. are also visible. The label design features blue and orange color bands with black text on a white background.*

FDA Label Image

Figure1 (Figure1)

Illustrations showing two methods of applying Diclofenac Sodium topical solution, either dispensing the liquid onto the palm of a hand for application or directly onto the skin of a knee. The images visually demonstrate possible application techniques for the topical medication.*

FDA Label Image

Figure2 (Figure2)

An instructional illustration showing a hand applying medication to the front of the knee. The image depicts arrows indicating the direction of application moving from the hand downward over the knee area.*

FDA Label Image

Figure3 (Figure3)

An instructional line drawing depicting a person applying ointment or gel to the back of their hand using the fingers of their other hand. The image suggests topical application of a medication, consistent with use instructions.*

FDA Label Image

Image Description (Varophen Packaging)

The packaging label for Varophen by Apotex Corp. presents Diclofenac Sodium Topical Solution, 1.5% (150 mL), and Muscle Rub Pain Relieving Cream, 3 oz. (85 grams). The label includes dosage forms, quantities, NDC 72835-201-02, storage instructions at 20°C to 25°C, and a barcode with recycling symbol. The design features the product name prominently with a geometric orange and red triangle pattern.*

FDA Label Image

Muscle Rub Image 1 (B5109d5c 7849 46b3 9bd6 44eac11ba556 01)

The packaging label for Perrigo Muscle Rub pain relieving cream, greaseless, in a 3 oz (85 g) tube. The label highlights deep penetrating pain relief for minor arthritis, backache, muscle, and joint pain. It includes the NDC 45802-174-53 and references coverage by FSA, HSA, and health plans. Distributed by Perrigo, Allegan, MI.*

FDA Label Image

Muscle Rub Image 2 (B5109d5c 7849 46b3 9bd6 44eac11ba556 02)

Drug Facts panel for Muscle Rub Greaseless Pain Relieving Cream listing active ingredients menthol 10% and methyl salicylate 15% as topical analgesics. It includes uses for minor aches and pains from simple backache, arthritis, strains, bruises, and sprains. Warnings indicate external use only and specific precautions. Directions advise application 3 to 4 times daily for adults and children over 12. Inactive ingredients and storage information are also provided.*

FDA Label Image

Structure (Structure)

Chemical structure of diclofenac sodium showing its molecular components including two chlorinated benzene rings connected by an amine group and a sodium carboxylate functional 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.