Bromhexine Hydrochloride Powder
Product Images NDC 51869-0009

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 Bromhexine Hydrochloride (NDC 51869-0009). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bidachem S.p.a., 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

Bromhexine1 (Bromhexine HCl 1)

Bromhexine1 (Bromhexine HCl 1)
Label for Bromhexine Hydrochloride bulk ingredient powder by Boehringer Ingelheim. The label shows material number 126958, batch number XXX, packing unit number 0001, and notes no temperature relevance for storage. Manufacturing and expiration dates are marked N/A.*
FDA Label Image

Bromhexine2 (Bromhexine HCl 2)

Bromhexine2 (Bromhexine HCl 2)
Safety and environmental warning text panel for Bromhexine Hydrochloride bulk ingredient powder. It includes hazard warnings that the substance is very toxic to aquatic life with long-lasting effects, instructions to avoid environmental release, to collect any spills, and to dispose of contents and container at an approved waste disposal plant. The text appears in Italian, German, and English, accompanied by an environmental hazard pictogram.*
FDA Label Image

Bromhexine3 (Bromhexine HCl 3)

Bromhexine3 (Bromhexine HCl 3)
Label for Bromhexine Hydrochloride powder, bulk ingredient, available in 1000 g strength. The label includes the NDC 518690009 and is marked for manufacturing, processing, or repacking, with prescription use only. Labeler is Bidachem S.p.a., affiliated with Boehringer Ingelheim.*

* 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.