Members Mark Arthritis Pain Reliever Gel
Product Images NDC 68196-523

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 26 technical images submitted to the FDA as part of the official labeling for Members Mark Arthritis Pain Reliever (NDC 68196-523). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sam's West 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

Leaflet Image 1 (Leaflet Image 1)

Leaflet Image 1 (Leaflet Image 1)
An instructional illustration showing two hands opening a box and removing a card or package insert. The image appears to demonstrate how to access the contents inside the box, likely for the MEMBERS MARK ARTHRITIS PAIN RELIEVER product packaging or accompanying informational material.*
FDA Label Image

Leaflet Image 10 (Leaflet Image 10)

Leaflet Image 10 (Leaflet Image 10)
An illustration showing a hand applying a topical gel onto the skin, demonstrating the method of use for a gel-based product*
FDA Label Image

Leaflet Image 11 (Leaflet Image 11)

Leaflet Image 11 (Leaflet Image 11)
An instructional illustration showing a person applying gel onto the back of the opposite hand, demonstrating topical use of a medication.*
FDA Label Image

Leaflet Image 12 (Leaflet Image 12)

Leaflet Image 12 (Leaflet Image 12)
An illustration showing hands demonstrating the application of topical gel. One hand is rubbing gel onto the back of the other hand's wrist, indicating method of topical use.*
FDA Label Image

Leaflet Image 13 (Leaflet Image 13)

Leaflet Image 13 (Leaflet Image 13)
An instructional illustration showing a hand applying topical gel to the front of a bent elbow area, likely demonstrating how to apply MEMBERS MARK 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 topical gel to the ankle area of a foot, demonstrating proper usage or application site for a topical gel product.*
FDA Label Image

Leaflet Image 15 (Leaflet Image 15)

Leaflet Image 15 (Leaflet Image 15)
An instructional diagram showing a hand applying gel to the top of a foot. The image demonstrates the topical application method for a gel product intended for external use on the foot area.*
FDA Label Image

Leaflet Image 16 (Leaflet Image 16)

Leaflet Image 16 (Leaflet Image 16)
An instructional illustration showing a person washing their hands under a running faucet with water splashing on the palms. The image emphasizes cleanliness or hand hygiene steps.*
FDA Label Image

Leaflet Image 17 (Leaflet Image 17)

Leaflet Image 17 (Leaflet Image 17)
An instructional line drawing showing hands holding a tube of topical gel under running water from a faucet. The label on the tube includes partial text referencing dosing for upper and lower body, and usage instructions, indicating it is a topical NSAID gel.*
FDA Label Image

Leaflet Image 18 (Leaflet Image 18)

Leaflet Image 18 (Leaflet Image 18)
An illustrated clock face showing 10 minutes, labeled with the text '10 minutes' inside the clock. The clock face has tick marks for minutes, and the time is highlighted in a shaded segment covering 10 minutes.*
FDA Label Image

Leaflet Image 19 (Leaflet Image 19)

Leaflet Image 19 (Leaflet Image 19)
An anatomical illustration comparing two joint cross-sections: one labeled 'Healthy cartilage' showing smooth cartilage between bones, and the other labeled 'Worn-away cartilage' showing rough, broken cartilage between bones, highlighting cartilage damage in a joint.*
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, indicating removal of the cap by twisting to access the contents. The image likely relates to the application or usage of a topical gel product.*
FDA Label Image

Leaflet Image 20 (Leaflet Image 20)

Leaflet Image 20 (Leaflet Image 20)
Illustration showing two images of an arm: the first depicts the palm side of an open hand with a star marking the center of the palm, and the second depicts a bent elbow with a star marking the inner elbow area. These likely indicate areas for topical application of a product.*
FDA Label Image

Leaflet Image 21 (Leaflet Image 21)

Leaflet Image 21 (Leaflet Image 21)
Illustration showing two grayscale images depicting topical application areas: one on the knee and one on the ankle/foot. Each area is marked with a star symbol indicating the site for applying the gel.*
FDA Label Image

Leaflet Image 22 (Leaflet Image 22)

Leaflet Image 22 (Leaflet Image 22)
An instructional illustration showing application sites for topical gel. The left panel depicts a hand with a star marking the area near the wrist. The right panel shows a side view of a foot with a star marking the area near the ankle.*
FDA Label Image

Leaflet Image 23 (Leaflet Image 23)

Leaflet Image 23 (Leaflet Image 23)
Instructional illustration showing two diagrams labeled "L" and "R" for left and right knees, respectively. Each diagram highlights the location of pain or arthritis in the knee joint with a star symbol. The diagrams are simple black and white graphics on a gray background.*
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 the sealed cap from the opening. The tube is held in the opposite hand, indicating the step for accessing the gel product inside.*
FDA Label Image

Leaflet Image 4 (Leaflet Image 4)

Leaflet Image 4 (Leaflet Image 4)
An instructional illustration showing a hand removing the cap by unscrewing it from a tube of MEMBERS MARK ARTHRITIS PAIN RELIEVER topical gel containing diclofenac sodium 10 mg/g.*
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 diagram illustrating proper and improper topical application areas on the body for a product. Correct applications include 2 areas such as hand and knee, or both knees, as well as 1 area such as one knee. An incorrect example shows 3 areas: both hands and one ankle, marked as improper.*
FDA Label Image

Dosing-card-lower (Dosing Card Lower)

Dosing-card-lower (Dosing Card Lower)
MEMBERS MARK ARTHRITIS PAIN RELIEVER Diclofenac Sodium topical gel tube, 1%, shown partially open. The dosage indicated for upper body use is 2.25 inches long (2 grams). Labeler is Sam's West Inc. The label includes application instructions relevant for dosing.*
FDA Label Image

Dosing-card-upper (Dosing Card Upper)

Dosing-card-upper (Dosing Card Upper)
An instructional illustration showing a hand squeezing MEMBERS MARK ARTHRITIS PAIN RELIEVER gel from a tube onto a dosing card. The card shows a measured line indicating a lower body dose of 4.5 inches long (4 grams). The tube cap is flipped open, and the gel is dispensed for topical application.*
FDA Label Image

Members-mark-arthritis-pain-reliever-carton-image.jpg (Members Mark Arthritis Pain Reliever Carton Image)

Members-mark-arthritis-pain-reliever-carton-image.jpg (Members Mark Arthritis Pain Reliever Carton Image)
MEMBERS MARK ARTHRITIS PAIN RELIEVER Diclofenac Sodium Topical Gel 1% (NSAID) is a medicated gel for topical use in arthritis pain relief. The packaging indicates it contains 3 tubes totaling 450 grams (15.87 oz). The labeler is Sam's West Inc, Bentonville, AR. It highlights anti-inflammatory use and daily arthritis pain treatment with external application only. The label includes drug facts, treatment areas illustrations, dosing card instructions, and warnings.*

* 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.