Bm Bm38 Drops Liquid
Product Images NDC 82969-2338

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bm Bm38 Drops (NDC 82969-2338). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Total Operations Management Llc Dba:bestmade Natural Products Micro, 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

Bm38 (Bm Bm38 (carton))

Bm38 (Bm   Bm38 (carton))
The packaging label for BM BM38 DROPS, a homeopathic liquid oral solution from Bestmade Natural Products. The front panel highlights its intended use for acne and pimples, including skin redness and irritation relief, with a net volume of 30 mL. The label lists multiple active ingredients in homeopathic dilutions and includes drug facts, warnings, directions, and contact information for the manufacturer, Total Operations Management LLC DBA Bestmade Natural Products Micro, with NDC 82969-2338.*
FDA Label Image

Bm38 (Bm Bm38 (label) Jpg)

Bm38 (Bm   Bm38 (label) Jpg)
Drug facts panel for BM BM38 DROPS, homeopathic liquid drops for acne and pimples, skin redness, and irritation. The panel lists uses, warnings, directions for use (10 drops with half a cup of water, 3-4 times daily for ages 12 and older), active ingredients with potencies, and inactive ingredient alcohol. Labeler information and net weight of 30 mL are also included.*
FDA Label Image

Bm38 (Bm Bm38 (pillow Box) Jpg)

Bm38 (Bm   Bm38 (pillow Box) Jpg)
BM BM38 Drops is a homeopathic liquid oral solution labeled for acne and pimples, including pimples, blemishes, skin redness, and irritation. The 30 mL bottle is marketed by Bestmade Natural Products Micro, a division of Total Operations Management LLC, located in Vero Beach, Florida. The label includes a Drug Facts panel listing active ingredients, uses, warnings, directions, and inactive ingredients. The NDC is 82969-2338-1.*

* 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.