Baczol Expectorant
Product Images NDC 76864-209

2 FDA label images from Procaps S.a. De C.v. · 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 Baczol Expectorant (NDC 76864-209). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Procaps S.a. De C.v., 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

209-02 Bacz Cart (209 02 Bacz Cart)

209-02 Bacz Cart (209 02 Bacz Cart)
Packaging label for BACZOL EXPECTORANT, a 4 fl oz (120 mL) liquid expectorant with fruit flavor, labeled by Procaps S.A. de C.V. The label is bilingual in English and Spanish, describing the product as a cough expectorant and nasal decongestant with active ingredient Guaifenesin 10 mg/mL. It includes directions to shake well before use, highlights the absence of sugar and alcohol, and provides usage instructions, warnings, and storage information. The label features an illustrative diagram of the respiratory system.*
FDA Label Image

209-02 Baczol Btl (209 02 Baczol Btl)

209-02 Baczol Btl (209 02 Baczol Btl)
Packaging label for BACZOL EXPECTORANT by Procaps S.A. de C.V. The product is a fruit-flavored liquid expectorant in a 4 fl. oz. (120 mL) bottle. It contains active ingredients including Guaifenesin 200 mg and Phenylephrine HCl 5 mg per 5 mL teaspoon. The label includes drug facts, warnings, usage instructions, storage conditions, and inactive ingredient information in English and Spanish.*

* 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.