Mqforu Pain Patch
Product Images NDC 83781-010

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Mqforu Pain Patch (NDC 83781-010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zhengzhou Miaoqi Medical Technology Co., Ltd., 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

1 (10)

Packaging label for Mqforu Pain Patch topical patch by Zhengzhou Miaoqi Medical Technology Co., Ltd. The front displays the brand name MQFORU and product name PAIN PATCH with a graphic of a tiger head and highlights 24 hours lasting relief. The box contains 10 patches sized 2.8 x 3.9 inches (7 x 10 cm). Drug Facts on the side list active ingredients menthol 2.0%, borneol 1.2%, and camphor 1.5% as topical analgesics, with usage warnings and directions included.*

FDA Label Image

7 (100)

Packaging label for MQFORU Pain Patch topical patch by Zhengzhou Miaoqi Medical Technology Co., Ltd. The front features a tiger illustration and highlights: 100 patches, 2.8 x 3.9 inches (7 x 10 cm) size, lasting up to 24 hours, comfortable flexible fabric, and easy to use and remove. The label includes active ingredients menthol 2.0%, borneol 1.2%, camphor 1.5%, and usage, warnings, directions, and inactive ingredients on the side panel.*

FDA Label Image

2 (20)

Packaging label for MQFORU Pain Patch, a topical OTC patch by Zhengzhou Miaoqi Medical Technology Co., Ltd. The label shows the brand name MQFORU prominently with 'PAIN PATCH' in large orange font. It includes a tiger illustration and highlights features like 24-hour lasting relief, comfortable flexible fabric, and ease of use. The package contains 20 patches, each sized 2.8 x 3.9 inches (7 x 10 cm). Drug facts with active ingredients menthol 2.0%, borneol 1.2%, and camphor 1.5% as topical analgesics are also listed.*

FDA Label Image

3 (30)

Packaging label for MQFORU Pain Patch, a topical patch available in a box containing 30 patches sized 2.8 by 3.9 inches. The label includes an image of a tiger and highlights features such as lasting up to 24 hours, comfortable flexible fabric, and ease of use and removal. Manufactured by Zhengzhou Miaoqi Medical Technology Co., Ltd, the label also displays Drug Facts with active ingredients menthol, borneol, and camphor, and includes usage directions and warnings.*

FDA Label Image

4 (40)

Packaging label for MQFORU Pain Patch, a topical pain patch for sore muscles, backaches, and joint pain. The box highlights 24-hour lasting effect, flexible fabric, and easy use and removal. The label includes a tiger illustration, specifies 40 patches of 2.8 x 3.9 inch size, and lists active ingredients menthol 2.0%, borneol 1.2%, and camphor 1.5%. Manufactured by Zhengzhou Miaoqi Medical Technology Co., Ltd. in China.*

FDA Label Image

5 (50)

Packaging label for MQFORU Pain Patch, a topical OTC pain relief patch by Zhengzhou Miaoqi Medical Technology Co., Ltd. The label features a bold orange and white design with a tiger graphic. It highlights the product's 24-hour lasting effect, flexible fabric, and ease of use. The box contains 50 patches measuring approximately 2.8 by 3.9 inches (7 cm by 10 cm). Drug facts and usage warnings are also printed on the packaging.*

FDA Label Image

6 (60)

Packaging label for Mqforu Pain Patch, a topical OTC pain patch by Zhengzhou Miaoqi Medical Technology Co., Ltd. The label highlights pain relief for sore muscles, backaches, and joint pain with 24-hour lasting effects. The package contains 60 patches sized 2.8 x 3.9 inches (7 x 10 cm) and features a tiger illustration. Active ingredients include menthol 2.0%, borneol 1.2%, and camphor 1.5%.*

* 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.