Diclofenac Sodium Kit
Product Images NDC 58602-606

Product Visual Gallery

This gallery contains 17 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 58602-606). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth 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

Figure 1 (Diclofenac Fig1)

An instructional illustration showing a person's hands opening a box and removing a blister card containing medication tablets. The image is related to Diclofenac Sodium 10 mg/g kit by Aurohealth LLC, demonstrating how to access the product within its packaging.*

FDA Label Image

Figure (Diclofenac Fig10)

An illustration showing two hands positioned under a faucet with water flowing, demonstrating hand washing technique in a sink area with tiled wall in the background.*

FDA Label Image

Figure (Diclofenac Fig11)

Illustration showing a person's hands holding and reading a tube of Diclofenac Sodium topical gel, 10 mg/g, near a sink with soap dispensers in the background, suggesting proper usage or hygiene instructions.*

FDA Label Image

Figure (Diclofenac Fig12)

Illustration showing a timer set to 10 minutes, likely indicating a timing instruction related to the product usage.*

FDA Label Image

Figure (Diclofenac Fig13)

An anatomical illustration comparing a healthy joint with normal cartilage to a joint with worn-away and broken cartilage. The diagram highlights the differences in cartilage condition between the two joints.*

FDA Label Image

Figure (Diclofenac Fig14)

Illustration showing body areas for application of Diclofenac Sodium topical kit. It includes labeled diagrams for upper body (hand and elbow), lower body (knee and ankle), combined upper/lower body (wrist and ankle), and specific lower body areas (left and right knee).*

FDA Label Image

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

This is a drug facts label for Diclofenac Sodium Topical Gel, 1% indicated as an NSAID arthritis pain reliever with anti-inflammatory properties. The label includes warnings about allergic reactions, liver damage, stomach bleeding, heart risks, and use during pregnancy or breastfeeding. It provides storage instructions, a contact number for questions, and distributor information for Aurohealth LLC. The net weight of the product is 3.53 oz (100 g).*

FDA Label Image

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

Diclofenac Sodium Topical Gel 1% kit packaging label by Aurohealth LLC. The box highlights its use as an NSAID arthritis pain reliever for areas including hand, wrist, elbow, foot, ankle, and knee. It includes dosing instructions and warnings, with a net weight of 3.53 oz (100 g).*

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 Aurohealth LLC. This OTC human drug kit is labeled for arthritis pain relief as an NSAID. The orange and blue label includes instructions for use, treatment areas such as hand, wrist, elbow, foot, ankle, and knee, and dosing guidance with a dosing card illustration. The net weight indicated is 2 x 150 g plus 50 g (350 g total).*

FDA Label Image

Figure (Diclofenac Fig2)

An instructional illustration showing two steps for opening a tube. Each frame depicts a hand twisting the cap counterclockwise to open the tube, with directional arrows indicating the motion. The tube is held in one hand while the other hand rotates the cap.*

FDA Label Image

Figure (Diclofenac Fig3)

An instructional illustration showing how to remove the protective cap from a tube by twisting it off with fingers. The image depicts two views of a tube with a screw-on cap being unscrewed, likely related to the Diclofenac Sodium 10 mg/g kit tube.*

FDA Label Image

Figure (Diclofenac Fig4)

Instructional illustrations showing how to twist open and close a cap on a tube, indicating hand positioning and rotational direction with arrows, likely related to the use of Diclofenac Sodium 10 mg/g topical kit.*

FDA Label Image

Figure (Diclofenac Fig5)

A sequence of four grayscale illustrations depicting various times 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 a setting sun, and end of the day with a crescent moon and clouds. Each scene is labeled accordingly.*

FDA Label Image

Figure (Diclofenac Fig6)

Instructional diagrams showing correct and incorrect application areas for Diclofenac Sodium topical use. Illustrations depict targeting areas on the hand, knee, knees, and ankle, with correct usage indicated for one or two areas and incorrect usage shown for three areas.*

FDA Label Image

Figure (Diclofenac Fig7)

An instructional illustration demonstrating the application of Diclofenac Sodium Topical Gel. It shows a hand dispensing gel from a tube onto a measuring strip labeled 'Lower body dose 4.5 inches long (0 grams)', indicating how to measure the appropriate amount of gel for use.*

FDA Label Image

Figure (Diclofenac Fig8)

Packaging label of Diclofenac Sodium Topical Gel, 1%, showing a tube with a dosing card inserted beneath it. The label indicates the gel's use for arthritis pain and notes the tube size as 2.25 inches (60 grams). The manufacturer is Aurohealth LLC.*

FDA Label Image

Figure (Diclofenac Fig9)

Illustrations showing application areas for a topical product on the body, divided into upper and lower body areas. The upper body areas include elbow, wrist, and hand; the lower body areas include knee, ankle, and foot. Each image depicts hands applying the product to various surfaces of the joints, with text detailing specific parts covered (e.g., sides, top, palm, fingers, kneecap, back, sole, 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.