Up And Up Arthritis Pain Reliever Gel
Product Images NDC 82442-251

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 27 technical images submitted to the FDA as part of the official labeling for Up And Up Arthritis Pain Reliever (NDC 82442-251). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Target Corporation, 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

Leaflet Image 1 (Leaflet Image 1)

Leaflet Image 1 (Leaflet Image 1)
An instructional illustration showing two hands, one holding an opened box and the other placing a product insert or medication package into it. The package appears to be rectangular with visible text blocks but no clear product name or dosage details.*
FDA Label Image

Leaflet Image 10 (Leaflet Image 10)

Leaflet Image 10 (Leaflet Image 10)
An illustration showing a hand applying topical gel to the inner elbow area, demonstrating the proper use of a topical gel product for arthritis pain relief.*
FDA Label Image

Leaflet Image 11 (Leaflet Image 11)

Leaflet Image 11 (Leaflet Image 11)
Illustration showing hands applying topical gel to the wrist area. One hand is rubbing gel onto the back of the other hand, demonstrating use of a topical gel product.*
FDA Label Image

Leaflet Image 12 (Leaflet Image 12)

Leaflet Image 12 (Leaflet Image 12)
An instructional illustration showing a pair of hands applying gel or cream, representing topical application. This image is likely associated with instructions for UP AND UP ARTHRITIS PAIN RELIEVER, a diclofenac sodium topical gel used for arthritis pain relief.*
FDA Label Image

Leaflet Image 13 (Leaflet Image 13)

Leaflet Image 13 (Leaflet Image 13)
An instructional illustration showing a hand applying topical gel onto the elbow area, suggesting the method of use for a topical arthritis pain reliever gel.*
FDA Label Image

Leaflet Image 14 (Leaflet Image 14)

Leaflet Image 14 (Leaflet Image 14)
An instructional illustration showing a hand applying gel to the ankle area of a foot. The image demonstrates topical application technique, likely for a medication such as UP AND UP ARTHRITIS PAIN RELIEVER gel.*
FDA Label Image

Leaflet Image 15 (Leaflet Image 15)

Leaflet Image 15 (Leaflet Image 15)
An instructional line drawing showing a hand applying topical gel to a foot, highlighting the use of a topical medication for pain relief in the foot area.*
FDA Label Image

Leaflet Image 16 (Leaflet Image 16)

Leaflet Image 16 (Leaflet Image 16)
An instructional illustration showing two hands being rinsed under running water from a faucet. Water droplets and streams are depicted flowing over the hands. The image likely depicts hand washing or rinsing technique.*
FDA Label Image

Leaflet Image 17 (Leaflet Image 17)

Leaflet Image 17 (Leaflet Image 17)
An instructional illustration showing two hands holding a medication tube under a running faucet. Water flows from the faucet onto the tube, presumably demonstrating how to wet the area or applicator before use. The tube label references gel dosage for upper body dose and shows a branded product name partially visible.*
FDA Label Image

Leaflet Image 18 (Leaflet Image 18)

Leaflet Image 18 (Leaflet Image 18)
An illustration of a clock face showing a highlighted 10-minute segment with the text '10 minutes' centered inside the clock. The image likely indicates a time-related instruction or waiting period.*
FDA Label Image

Leaflet Image 19 (Leaflet Image 19)

Leaflet Image 19 (Leaflet Image 19)
Illustration comparing healthy cartilage and worn-away cartilage in a joint. The healthy cartilage illustration shows smooth, intact cartilage, while the worn-away cartilage illustration depicts broken cartilage and bone surfaces, highlighting joint deterioration.*
FDA Label Image

Leaflet Image 2 (Leaflet Image 2)

Leaflet Image 2 (Leaflet Image 2)
An instructional illustration showing hands opening the cap of a tube, with arrows indicating the direction to twist the cap counterclockwise and pull it off the tube.*
FDA Label Image

Leaflet Image 20 (Leaflet Image 20)

Leaflet Image 20 (Leaflet Image 20)
Illustration showing the application areas for UP AND UP ARTHRITIS PAIN RELIEVER gel. The left panel depicts the star marking the center of the palm, and the right panel depicts the star marking the inner elbow area.*
FDA Label Image

Leaflet Image 21 (Leaflet Image 21)

Leaflet Image 21 (Leaflet Image 21)
Illustration showing application areas for UP AND UP ARTHRITIS PAIN RELIEVER gel, specifically the knee and ankle regions, indicated by black star marks on simplified human limb drawings.*
FDA Label Image

Leaflet Image 22 (Leaflet Image 22)

Leaflet Image 22 (Leaflet Image 22)
Illustration showing application areas for a topical gel with stars marking the wrist and ankle, indicating likely locations for product use on joints or arthritis pain.*
FDA Label Image

Leaflet Image 23 (Leaflet Image 23)

Leaflet Image 23 (Leaflet Image 23)
An instructional illustration showing two knee diagrams labeled 'L' for left and 'R' for right, each with a star marking a specific area on the front of the knee joint, likely indicating application sites for the topical gel.*
FDA Label Image

Leaflet Image 3 (Leaflet Image 3)

Leaflet Image 3 (Leaflet Image 3)
An instructional illustration showing a hand opening a tube by twisting off a seal from the tube's opening. The image demonstrates how to remove the safety seal before using the product.*
FDA Label Image

Leaflet Image 4 (Leaflet Image 4)

Leaflet Image 4 (Leaflet Image 4)
An instructional illustration showing hands opening a tube by twisting the cap to remove it, revealing the tube opening. This likely demonstrates how to open the tube of UP AND UP ARTHRITIS PAIN RELIEVER gel for topical application.*
FDA Label Image

Leaflet Image 5 (Leaflet Image 5.0.jpg)

FDA Label Image

Leaflet Image 5.1 (Leaflet Image 5.1.jpg)

FDA Label Image

Leaflet Image 6 (Leaflet Image 6.0.jpg)

FDA Label Image

Leaflet Image 6.1 (Leaflet Image 6.1.jpg)

FDA Label Image

Leaflet Image 7 (Leaflet Image 7)

Leaflet Image 7 (Leaflet Image 7)
An instructional illustration showing correct and incorrect examples of body areas for topical application, highlighting hands, knees, ankles with labels. It indicates that applying to 1 or 2 areas (hand and knee; knees; or knee alone) is correct, while applying to 3 areas (hands and ankle) is incorrect.*
FDA Label Image

Dosing-card-lower (Dosing Card Lower)

Dosing-card-lower (Dosing Card Lower)
The image shows a dosing card for Diclofenac Sodium Topical Gel 1%, an NSAID, indicated for upper body dose measurement (2.25 inches long, 2 grams). The card is white with black and gray text, used for measuring gel application amount. The label includes usage instructions and precaution to read the product use guide.*
FDA Label Image

Dosing-card-upper (Dosing Card Upper)

Dosing-card-upper (Dosing Card Upper)
An instructional illustration showing a hand squeezing a tube of topical gel onto a dosing card. The dosing card indicates measurement details for applying a lower body dose, specifically 4.5 inches long (4 grams) of gel. The tube is labeled with the generic name Diclofenac Sodium.*
FDA Label Image

Up&up-arthritis-pain-reliever-carton-image-1.jpg (Image 01)

Up&up-arthritis-pain-reliever-carton-image-1.jpg (Image 01)
Packaging label for UP AND UP ARTHRITIS PAIN RELIEVER Topical Gel 10 mg/g (1%) containing Diclofenac Sodium. The 150 g tube is indicated for topical use to relieve arthritis pain and inflammation. The label highlights treatment areas including knee, foot/ankle, elbow, and hand/wrist, and includes dosing instructions and safety information. Manufactured by Target Corporation.*
FDA Label Image

Up&up-arthritis-pain-reliever-carton-image-2.jpg (Image 02)

Up&up-arthritis-pain-reliever-carton-image-2.jpg (Image 02)
Drug Facts text panel for UP AND UP ARTHRITIS PAIN RELIEVER Diclofenac Sodium Gel 1%. Includes active ingredient, uses for arthritis pain relief in specific areas, warnings about allergies and side effects, directions for use up to 21 days, and storage information. Also provides cautionary notes about heart attack, stroke risks, and advice to ask a doctor before use under certain conditions. Includes instructions for dose measurement and contact information for questions.*

* 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.