Diclofenac Sodium Gel
Product Images NDC 67296-2155

Product Visual Gallery

This gallery contains 17 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 67296-2155). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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)

An illustration depicting a person's hands opening a carton and removing a rectangular medication package, suggesting the action of accessing the drug product for use or inspection.*

FDA Label Image

Figure (Diclofenac Fig10)

An illustration showing two hands washing under a faucet with running water and two soap dispensers mounted on a tiled wall. The image depicts hand hygiene practices.*

FDA Label Image

Figure (Diclofenac Fig11)

An instructional illustration depicting a person holding a small tube of topical medication, likely Diclofenac Sodium gel, with both hands. The background suggests a bathroom sink area with visible soap or lotion dispensers mounted on a tiled wall, indicating the setting for applying the topical gel.*

FDA Label Image

Figure (Diclofenac Fig12)

Illustration depicting a timer set to 10 minutes on a rectangular background with rounded edges. The timer display shows the text '10 minutes' in bold black font inside a circular dial.*

FDA Label Image

Figure (Diclofenac Fig13)

An anatomical illustration comparing healthy cartilage with damaged cartilage. The left side shows normal, healthy cartilage within a joint, while the right side depicts worn-away and broken cartilage, indicating cartilage deterioration or damage.*

FDA Label Image

Figure (Diclofenac Fig14)

Illustrations depicting common application sites for a topical gel: upper body (hand and elbow), lower body (knee and ankle), combined upper/lower body (wrist and ankle), and lower body with left and right knees indicated separately. Each illustration highlights specific joints for topical use.*

FDA Label Image

Package Label-principal Display Panel (1% w/w tube Label (100 g Bottle))

Label for Diclofenac Sodium Topical Gel, 1%, a 100 g tube for arthritis pain. The label highlights NSAID anti-inflammatory action, external use only, and warnings including allergy, stomach bleeding, heart attack, and stroke risks. It is distributed by Aurohealth LLC and is labeled for original prescription strength.*

FDA Label Image

Package Label-principal Display Panel (1% w/w Container Carton Label (100 g Bottle))

Diclofenac Sodium Topical Gel, 1%, by Redpharm Drug, is an NSAID arthritis pain reliever in gel form for topical use. The label highlights treatment areas including hand, wrist, elbow, foot, ankle, and knee. The net weight is 3.53 oz (100 g), with dosing instructions and Drug Facts on the packaging. The label features an orange and blue design with the AUROHEALTH logo.*

FDA Label Image

Package Label-principal Display Panel (1% w/w Tube Carton Label (350 g tube))

Packaging label for Diclofenac Sodium Topical Gel, 1%, by Redpharm Drug, containing 2 x 150 g + 50 g (350 g total). The orange and blue box highlights its use as an arthritis pain reliever NSAID for topical application, specifying treatment areas like hand, wrist, elbow, foot, ankle, and knee. The label includes dosing instructions, usage directions, and safety information.*

FDA Label Image

Figure (Diclofenac Fig2)

Illustration showing hands opening a tube cap by twisting it counterclockwise, demonstrating how to open the tube containing the topical gel.*

FDA Label Image

Figure (Diclofenac Fig3)

An instructional illustration showing a hand removing the cap from a tube, with arrows indicating the direction to pull the cap away from the tube opening.*

FDA Label Image

Figure (Diclofenac Fig4)

Two-step instructional diagram showing how to open a tube cap. The first step illustrates applying downward pressure and turning the cap to break the seal. The second step depicts the full removal of the cap by turning it further. The images use arrows to indicate the movement direction.*

FDA Label Image

Figure (Diclofenac Fig5)

An instructional illustration showing four phases of the day: start of the day with a rising sun, middle of the day with the sun high in the sky, late afternoon with the sun low near the horizon, and end of the day with a moon in a cloudy night sky. The sequence likely indicates timing guidance related to the use of Diclofenac Sodium 10 mg/g topical gel by Redpharm Drug.*

FDA Label Image

Figure (Diclofenac Fig6)

An instructional diagram illustrating the correct and incorrect application areas for a topical gel. It shows multiple human body silhouettes highlighting hands, knees, and ankle areas. Correct applications involve one or two designated areas, whereas applying to three areas is marked as incorrect.*

FDA Label Image

Figure (Diclofenac Fig7)

An instructional illustration showing a hand applying Diclofenac Sodium topical gel from a tube onto a measured dosing strip. The strip indicates a dose of 4.5 inches (or grams) for treating a lower body area, demonstrating the recommended application amount.*

FDA Label Image

Figure (Diclofenac Fig8)

Diclofenac Sodium Topical Gel 1% in a tube with a dispensing tip. The label shows instructions to apply the gel dose of 2.25 inches (equivalent measurement in grams), indicating it is used for arthritis pain relief. The tube is partially squeezed to dispense the gel.*

FDA Label Image

Figure (Diclofenac Fig9)

An instructional diagram showing application areas for topical gel on upper and lower body parts. It illustrates applying gel to elbow, wrist, and hand on the upper body and to knee, ankle, and foot on the lower body, highlighting the relevant surfaces such as sides, tops, bottoms, palms, fingers, kneecap, sole, and toes.*

* 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.