Up And Up Arthritis Pain Reliever Gel
Product Images NDC 11673-569

Product Visual Gallery

This gallery contains 16 technical images submitted to the FDA as part of the official labeling for Up And Up Arthritis Pain Reliever (NDC 11673-569). 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

Apply To Areas (Apply To Areas)

Illustration showing application areas for topical use of up and up arthritis pain reliever gel on the upper and lower body. It includes labeled diagrams for elbow, wrist, and hand on the upper body, and knee, ankle, and foot on the lower body, highlighting specific regions where the gel can be applied.*

FDA Label Image

Hands Opening Package (Hands Opening Package)

An instructional illustration depicting a person's hands opening a carton and removing a blister card containing multiple gel packets, indicating the packaging format of the up and up arthritis pain reliever topical gel.*

FDA Label Image

Opening Tube (Opening Tube)

An instructional black and white line drawing showing two hands opening a tube by twisting and pulling off the cap. The tube is held in one hand, while the other hand grasps the cap with an arrow indicating to twist and pull it off.*

FDA Label Image

Remove Cap (Remove Cap)

An instructional illustration showing how to remove the cap from a tube by twisting it off, likely part of directions for using a topical gel product such as an arthritis pain reliever.*

FDA Label Image

Replace Cap (Replace Cap)

An instructional black-and-white line drawing showing a person twisting the cap off a tube, demonstrating how to open the tube container.*

FDA Label Image

Cartilage (Cartilage)

An anatomical illustration showing a comparison between a healthy joint with intact cartilage and a joint with worn-away cartilage. The worn cartilage area is labeled, highlighting broken cartilage within the joint space.*

FDA Label Image

Correct Examples (Correct Examples)

An instructional diagram showing application sites for up and up arthritis pain reliever gel. It highlights areas on the upper body (hand and elbow), lower body (knees and ankle), upper/lower body (wrist and ankle), and specifically the left and right knees for topical use.*

FDA Label Image

Where To Apply (Examples Of Where To Apply)

An instructional diagram showing correct and incorrect application areas for topical gel. It depicts body outlines with labeled regions such as hand, knee, knees, ankles, and hands. It indicates 1 to 2 correct application areas versus an incorrect use on three areas at once.*

FDA Label Image

How Often To Use (Four Times A Day)

An illustration showing four time-of-day icons labeled as Start of the day (sunrise), Middle of the day (sun high), Late afternoon (sun low), and End of the day (crescent moon). This diagram likely indicates timing or frequency related to product use.*

FDA Label Image

Arthritis Pain Reliever Image (Image 01)

up & up arthritis pain reliever diclofenac sodium topical gel 1%, 150 g tube label. The orange and white label states it is for arthritis pain relief, anti-inflammatory, and external use only. It compares to Voltaren Arthritis Pain and shows dosing instructions with an enclosed card. Treatment areas include hand, wrist, elbow, foot, ankle, and knee. Labeler is Target Corporation.*

FDA Label Image

Image 02

Drug Facts for up and up arthritis pain reliever 10 mg/g gel with active ingredient diclofenac sodium 1%. The panel covers active ingredients, uses for temporary arthritis pain relief, warnings including allergy risk, liver and stomach warnings, usage directions, storage instructions, and additional safety information. The label advises using the enclosed dosing card and contains a customer support phone number.*

FDA Label Image

Measure Using Dosing Card (Measure Using Dosing Card 2)

An instructional illustration showing a tube of Diclofenac Sodium Topical Gel, 1%, with a dosing card indicating application for the upper body dose of 2.25 inches (about 2 grams). The image also includes a note to read the product user guide before use and states that it is not for immediate pain relief.*

FDA Label Image

Measure Using Dosing Card (Measure Using Dosing Card)

Illustration showing a hand dispensing up and up arthritis pain reliever gel, diclofenac sodium 10 mg/g, from a tube onto a dosing card. The card includes a marked area labeled for a lower body dose of 4.5 grams and advises reading the product Use Guide before use, noting it is not for immediate pain relief.*

FDA Label Image

Wait 10 Minutes (Wait 10 Minutes)

An illustration of a circular clock face showing 10 minutes, with the labeled text '10 minutes' inside the clock. The shaded segment highlights the initial 10-minute portion of the clock, indicating a time interval.*

FDA Label Image

Wash The Dosing Card (Wash The Dosing Card)

Illustration showing a person holding an up and up arthritis pain reliever card under running water, demonstrating the proper way to wash or clean the product label or card.*

FDA Label Image

Wash Your Hands (Wash Your Hands)

An instructional black and white line drawing showing a pair of hands rinsing under running water, likely demonstrating proper hand washing or cleaning technique before or after applying a product.*

* 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.