Arthritis Pain Reliever Gel
Product Images NDC 56062-878

16 FDA label images from Publix Super Markets Inc · 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 Arthritis Pain Reliever (NDC 56062-878). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Publix Super Markets 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

Arthritis Pain Reliver Image (Image 01)

Arthritis Pain Reliver Image (Image 01)
The packaging label for Arthritis Pain Reliever diclofenac sodium topical gel 1%, original prescription strength, 3.53 oz (100 g) by Publix Super Markets Inc. The label highlights the product as a medicated gel for arthritis pain relief used on the hand, wrist, elbow, foot, ankle, and knee. It includes dosing instructions with an enclosed dosing card and usage guidelines for topical application. The label cautions for external use only and features a barcode and distributor information.*
FDA Label Image

Dicolfenac-image1 (Image 02)

Dicolfenac-image1 (Image 02)
An instructional illustration depicting a hand removing a rectangular product box from a larger open container. The image shows two hands; one holding the box and the other lifting the smaller box out, without visible text details on the box.*
FDA Label Image

Image 2 (Image 03)

Image 2 (Image 03)
An instructional line drawing showing how to open a tube by twisting and pulling off the cap. This likely relates to preparing a topical gel for use.*
FDA Label Image

Image 3 (Image 04)

Image 3 (Image 04)
An instructional illustration showing hands removing the cap from a tube, indicating the arrow direction to unscrew or pull off the cap. This visual likely pertains to the opening or usage instructions for a topical gel product.*
FDA Label Image

Image 4 (Image 05)

Image 4 (Image 05)
An instructional illustration showing hands opening a tube by unscrewing the cap, with an arrow indicating the motion to remove the cap. The tube is intended to contain a topical gel product.*
FDA Label Image

Image 5 (Image 06)

Image 5 (Image 06)
Illustration showing four panels representing different times of day: start of the day with a rising sun, middle of the day with a high sun, late afternoon with a setting sun, and end of the day with a crescent moon. The images likely depict timing related to product use or daily routine.*
FDA Label Image

Image 6 (Image 07)

Image 6 (Image 07)
An instructional diagram showing correct and incorrect application areas for a topical gel. Four figures indicate labeled body parts such as hand, knee, knees, hands, and ankle, demonstrating examples with checkmarks for correct application (1 or 2 areas) and an X mark for incorrect application covering 3 areas.*
FDA Label Image

Diclofenac-graphic2 (Image 08)

Diclofenac-graphic2 (Image 08)
An instructional diagram showing a hand holding a dosing card for topical gel application. The dosing card is labeled for use with diclofenac sodium gel and indicates a lower body dose of 4.5 inches long (8 grams).*
FDA Label Image

Diclofenac-graphic3 (Image 09)

Diclofenac-graphic3 (Image 09)
The image shows a dosing card for Diclofenac Sodium Topical Gel, 1% (10 mg/g), branded as arthritis pain reliever. The label includes dosing instructions for upper body use, specifying 2 grams per dose. The product is manufactured by Perrigo and intended for topical application.*
FDA Label Image

Image 9 (Image 10)

Image 9 (Image 10)
Illustrative diagram showing application areas for arthritis pain reliever gel on upper and lower body areas. It highlights the elbow (including sides, inner, and outer), wrist (sides, top, bottom), and hand (top, palm, fingers) on the upper body, and the knee (sides, kneecap, back), ankle (sides, front, back), and foot (sole, top, toes) on the lower body.*
FDA Label Image

Image 10 (Image 11)

Image 10 (Image 11)
An instructional illustration showing water flowing from a faucet onto hands being washed. The image depicts proper handwashing technique by rinsing under running water, with droplets visible around the hands.*
FDA Label Image

Diclofenac-graphic4 (Image 12)

Diclofenac-graphic4 (Image 12)
An instructional illustration showing hands holding an arthritis pain reliever gel tube under running water, likely depicting how to clean the hands or tube after use.*
FDA Label Image

Image 12 (Image 13)

Image 12 (Image 13)
An illustration of a clock face showing 10 minutes, with the shaded area representing 10 minutes. This figure is likely used to indicate the duration related to the product's use or effect timing.*
FDA Label Image

Image 13 (Image 14)

Image 13 (Image 14)
An illustration showing two side-by-side diagrams of a knee joint. The left diagram depicts a healthy knee joint with intact cartilage. The right diagram shows a knee joint with worn-away and broken cartilage, indicating cartilage degradation around the joint surfaces.*
FDA Label Image

Image 14 (Image 15)

Image 14 (Image 15)
Illustration showing body areas for topical application of arthritis pain reliever gel. Depicts hand and elbow (upper body), knees and ankle (lower body), wrist and ankle, and both left and right knees as targeted sites for use.*
FDA Label Image

Image 16

Image 16
Drug Facts panel for arthritis pain reliever gel containing diclofenac sodium 1% topical NSAID. The text includes active ingredient identification, uses for arthritis pain relief, warnings for allergy and adverse reactions, detailed precautions, directions for use, storage instructions, and a list of inactive ingredients including polymers and solvents. Dosage and safety information for specific populations are included.*

* 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.