Diclofenac Sodium Gel
Product Images NDC 73581-922

17 FDA label images from Yyba Corp · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 17 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 73581-922). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Yyba Corp, 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

Figure 1 (Diclofenac Fig1)

Figure 1 (Diclofenac Fig1)
An instructional illustration showing hands opening a box and removing a single strip or packet of medication, demonstrating how to access the product packaging inside.*
FDA Label Image

Figure (Diclofenac Fig2)

Figure (Diclofenac Fig2)
Instructional illustrations showing how to open a tube cap. The images depict a hand gripping a small tube and turning the cap counterclockwise to remove it. The tube is held horizontally, and arrows indicate the direction of rotation for opening.*
FDA Label Image

Figure (Diclofenac Fig3)

Figure (Diclofenac Fig3)
Instructional line art illustrations showing two steps to open a tube: the first image depicts removing a cap from a tube, and the second image shows removing a seal or foil from the tube opening. These illustrations are likely related to proper usage of the Diclofenac Sodium topical gel.*
FDA Label Image

Figure (Diclofenac Fig4)

Figure (Diclofenac Fig4)
Instructional illustration showing how to open and close the cap of a tube, likely for topical gel application. The images depict hands twisting the cap to either open the tube or close it, with arrows indicating the direction of rotation.*
FDA Label Image

Figure (Diclofenac Fig5)

Figure (Diclofenac Fig5)
A series of four grayscale illustrations depicting times of day: start of the day (sunrise), middle of the day (sun overhead), late afternoon (sun low on horizon), and end of the day (nighttime with crescent moon and clouds). Each is labeled accordingly.*
FDA Label Image

Figure (Diclofenac Fig6)

Figure (Diclofenac Fig6)
An instructional diagram depicting correct and incorrect topical application areas for a topical gel. The illustrations show the human body with marked areas: hand and knee (correct, 2 areas), knees (correct, 2 areas), knee (correct, 1 area), and hands and ankle (incorrect, 3 areas).*
FDA Label Image

Figure (Diclofenac Fig7)

Figure (Diclofenac Fig7)
An instructional illustration showing a hand applying Diclofenac Sodium Topical Gel from a tube onto a designated marked area on the skin, indicated as the application site for localized arthritis pain relief, with a note to use the product as directed.*
FDA Label Image

Figure (Diclofenac Fig8)

Figure (Diclofenac Fig8)
Diclofenac Sodium Topical Gel 1% in a tube with a dosing card overlay. The label states the product is for arthritis pain relief and provides instructions on how to apply a specific daily dose length from the gel tube. The labeler is YYBA CORP.*
FDA Label Image

Figure (Diclofenac Fig9)

Figure (Diclofenac Fig9)
Illustrations showing topical application areas of Diclofenac Sodium gel on upper and lower body parts. Depicted are the elbow, wrist, and hand in the upper body areas, and the knee, ankle, and foot in the lower body areas, with arrows indicating where to apply the gel, including sides, front, back, palm, fingers, toes, and soles as appropriate.*
FDA Label Image

Figure (Diclofenac Fig10)

Figure (Diclofenac Fig10)
An illustration showing a person washing their hands with soap and water at a sink with two soap dispensers. The image likely demonstrates proper hand hygiene or hand washing steps.*
FDA Label Image

Figure (Diclofenac Fig11)

Figure (Diclofenac Fig11)
An illustration showing hands holding a tube of Diclofenac Sodium gel 10 mg/g, demonstrating the application method or dispensing from the tube. The background includes a sink with soap dispensers, indicating a focus on proper hygiene or usage instructions for this topical gel product.*
FDA Label Image

Figure (Diclofenac Fig12)

Figure (Diclofenac Fig12)
An illustration of a timer or clock showing "10 minutes" prominently in the center. The design is circular, resembling a stopwatch face, with minute marks around the edge.*
FDA Label Image

Figure (Diclofenac Fig13)

Figure (Diclofenac Fig13)
An anatomical diagram showing two knee joints side-by-side. The left joint depicts healthy cartilage with a smooth, intact surface. The right joint shows worn-away and broken cartilage, indicating damage or degradation of the joint surface.*
FDA Label Image

Figure (Diclofenac Fig14)

Figure (Diclofenac Fig14)
Illustrations showing recommended topical application sites for Diclofenac Sodium 10 mg/g gel. They depict locations on the upper body (hand and elbow), lower body (knee and ankle), combined upper/lower body (wrist and ankle), and lower body focusing on left and right knees.*
FDA Label Image

Tube (Screenshot 2026 10 13 170323)

Tube (Screenshot 2026 10 13 170323)
Diclofenac Sodium Topical Gel, 1% strength, in a 3.53 oz (100 g) tube container. The label designates it as an NSAID arthritis pain reliever for external use only and includes warnings, usage instructions, and storage information. The labeler is YYBA CORP.*
FDA Label Image

Tube (Diclo)

Tube (Diclo)
Diclofenac Sodium Topical Gel 1%, 10 mg/g strength, is shown in a flat carton packaging label. The label indicates it is a medicated gel used for arthritis pain relief, labeled as original prescription strength. The labeler is YYBA Corp. The package includes dosing instructions, treatment areas illustrations, and a barcode.*
FDA Label Image

1 (Screenshot 2026 10 13 164500)

1 (Screenshot 2026 10 13 164500)
Drug Facts label panels providing active ingredient information, warnings, directions, and other consumer guidance for Diclofenac Sodium topical gel 10 mg/g. The text is formatted in sections with bullet points outlining precautions, usage instructions, and adverse reactions.*

* 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.