Diclofenac Sodium Gel
Product Images NDC 57483-185

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 16 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 57483-185). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Innovus Pharmaceuticals, Inc., 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 illustration showing hands opening a carton box and removing a single strip of medication blister packaging. The image demonstrates how to take the product out of its carton container, likely related to the DICLOFENAC SODIUM topical gel product packaging.*
FDA Label Image

Figure (Diclofenac Fig10)

Figure (Diclofenac Fig10)
An instructional illustration depicts hands applying gel to another hand under a faucet, suggesting topical application and handwashing instructions related to product use.*
FDA Label Image

Figure (Diclofenac Fig11)

Figure (Diclofenac Fig11)
Illustration showing a person holding and squeezing a tube of DICLOFENAC SODIUM 10 mg/g topical gel over a sink, demonstrating dosage application instructions.*
FDA Label Image

Figure (Diclofenac Fig12)

Figure (Diclofenac Fig12)
Illustration of a timer or stopwatch showing 10 minutes prominently displayed in the center, likely indicating a time duration related to product use or instructions.*
FDA Label Image

Figure (Diclofenac Fig13)

Figure (Diclofenac Fig13)
An anatomical illustration showing a comparison between a healthy joint with intact cartilage and a joint with worn-away and broken cartilage, highlighting cartilage degradation.*
FDA Label Image

Figure (Diclofenac Fig14)

Figure (Diclofenac Fig14)
An instructional diagram showing four illustrated sections of the body labeled for topical application of medication. The sections include upper body (hand and elbow), lower body (knee and ankle), upper/lower body (wrist and ankle), and lower body with left and right knee highlighted.*
FDA Label Image

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

Package Label-principal Display Panel (1% w/w tube Label (100 g Bottle))
Packaging label for Diclofenac Sodium Topical Gel, 1% by Innovus Pharmaceuticals, Inc. The label identifies it as an NSAID arthritis pain reliever in a 5.29 oz (150 g) tube. Instructions for opening, warnings, usage precautions, and storage information are included, along with distributor contact details and a barcode.*
FDA Label Image

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

Package Label-principal Display Panel (1% w/w Container Carton Label (100 g Bottle))
Packaging label for Diclofenac Sodium Topical Gel, 1% by Innovus Pharmaceuticals, Inc. It is a medicated gel indicated as an arthritis pain reliever and anti-inflammatory. The label lists treatment areas including hand, wrist, elbow, foot, ankle, and knee, with usage instructions and dosing card guidance for upper and lower body doses. The net weight is 5.29 oz (150 g).*
FDA Label Image

Figure (Diclofenac Fig2)

Figure (Diclofenac Fig2)
Instructional illustration showing hands removing a cap from a tube by twisting it counterclockwise. The image consists of two panels demonstrating the cap removal process, likely for a topical gel product such as diclofenac sodium gel.*
FDA Label Image

Figure (Diclofenac Fig3)

Figure (Diclofenac Fig3)
Instructional illustration showing a person removing the cap from a tube by twisting it counterclockwise. Two similar images depict the step of opening the tube, likely indicating preparation for applying topical gel.*
FDA Label Image

Figure (Diclofenac Fig4)

Figure (Diclofenac Fig4)
Two black-and-white instructional illustrations showing the steps to open a tube by twisting its cap counterclockwise. Both images focus on hands holding the tube and rotating the cap as indicated by arrows.*
FDA Label Image

Figure (Diclofenac Fig5)

Figure (Diclofenac Fig5)
An instructional illustration showing four panels depicting times of day: start of the day with a rising sun, middle of the day with the sun overhead, late afternoon with the sun low on the horizon, and end of the day with a crescent moon in a night sky with clouds.*
FDA Label Image

Figure (Diclofenac Fig6)

Figure (Diclofenac Fig6)
An instructional diagram illustrating the correct and incorrect application areas for topical gel. It shows human body silhouettes with specific body parts (hand, knee, knees, ankle) marked to indicate where the gel may be applied correctly (1 or 2 areas) and incorrectly (3 areas).*
FDA Label Image

Figure (Diclofenac Fig7)

Figure (Diclofenac Fig7)
An instructional illustration showing a hand dispensing diclofenac sodium topical gel from a tube onto a measuring strip. The strip is marked to measure an accurate dose of gel for application, supporting proper usage guidance for diclofenac sodium topical gel.*
FDA Label Image

Figure (Diclofenac Fig8)

Figure (Diclofenac Fig8)
DICLOFENAC SODIUM topical gel tube label showing 1% strength, indicated for arthritis pain relief. The label includes application instructions to apply a specific dose and a dosing card guide. The tube is partially squeezed to display the gel's use. Labeler information is not visible in the image.*
FDA Label Image

Figure (Diclofenac Fig9)

Figure (Diclofenac Fig9)
Illustrations showing how to apply Diclofenac Sodium gel 10 mg/g topical medication on various upper and lower body areas. It includes depicted application on the elbow (sides, inner, outer), wrist (sides, top, bottom), hand (top, palm, fingers), knee (sides, kneecap, back), ankle (sides, front, back), and foot (sole, top, toes). Each area is demonstrated with hand motions indicating gel application.*

* 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.