Doitu Acne Microcrystalline Invisible Acne Patch
Product Images NDC 83093-102

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Doitu Acne Microcrystalline Invisible Acne Patch (NDC 83093-102). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Guangdong Zhizhen Biological Medicine 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

Label Version 1 (Doitu Patch(0.05gx36) V1)

Label Version 1 (Doitu Patch(0.05gx36) V1)
Doitu acne microcrystalline invisible acne patch packaging label showing a black and orange box design. The front panel states the product name with a count of 36 stickers and net content of 0.05g per sticker. The back panel includes drug facts with active ingredients like Salix alba bark extract, menthol, and others for acne treatment, usage instructions, warnings, directions, and storage information. It lists Guangdong ZhiZhen Biological Medicine Co., Ltd. as the manufacturer.*
FDA Label Image

Label Version 2 (Doitu Patch(0.05gx36) V2)

Label Version 2 (Doitu Patch(0.05gx36) V2)
Doitu acne microcrystalline invisible acne patch packaging label featuring 36 stickers. The front displays the product name along with net content (0.05g/sticker × 36 stickers) and the labeler Guangdong ZhiZhen Biological Medicine Co., Ltd. The back panel includes a Drug Facts box detailing active ingredients such as Salix alba bark extract and menthol, usage instructions, warnings, directions, and manufacturer information. The package is marked as homeopathic and made in China.*

* 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.