Bronchi-pertu Syrup
Product Images NDC 59469-303

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Bronchi-pertu (NDC 59469-303). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pekana Naturheilmittel Gmbh, 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

Principal Display Panel (125 ml Bottle Box)

BRONCHI-PERTU homeopathic drops syrup carton label for a 4.25 FL OZ (125 ml) bottle, distributed by BioResource Inc. and manufactured by PEKANA GmbH. The label lists ingredients including Bryonia cretica, Dactylopisus coccus, Grindelia robusta, Guaiacum, and others, with 21% alcohol by volume. It is identified as an antitussive expectorant with usage indications and warnings provided. The NDC code is 59469-303-20.*

FDA Label Image

Principal Display Panel (250 ml Bottle Box)

BRONCHI-PERTU Homeopathic Drops Syrup 8.5 fl. oz. (250 ml) packaging label shows it as an antitussive expectorant homeopathic medicine. The label lists active homeopathic ingredients like Bryonia cretica, Dactylopis coccus, Grindelia robusta, Guaiacum, and others. Manufactured by PEKANA GmbH and distributed by BioResource Inc in Cotati, CA, USA. Contains 21% alcohol by volume.*

* 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.