Goyescas 7 Syrups Alcohol And Sugar Free
Product Images NDC 11856-0031

2 FDA label images from Goyescas Of Fla · 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 Goyescas 7 Syrups Alcohol And Sugar Free (NDC 11856-0031). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Goyescas Of Fla, 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

Carton (Goyescas 7 Syrups Alcohol And Sugar Free 6 Oz. Carton 001)

Carton (Goyescas 7 Syrups Alcohol And Sugar Free 6 Oz. Carton 001)
The image shows the unfolded carton for Goyescas 7 Syrups Alcohol and Sugar Free Cough and Cold. The packaging features a tan background with repeated seals stating "Goyescas Made in USA Corporation." The front panel highlights the product name, "Goyescas 7 Syrups," and indicates it is alcohol and sugar free. Active ingredients and drug facts are listed, including Dextromethorphan HBr, Guaifenesin, and Phenylephrine HCl. The labeler is GOYESCAS CORP., Miami, Florida, and the net contents indicated are 6 fluid ounces.*
FDA Label Image

Label (Goyescas 7 Syrups Alcohol And Sugar Free 6 Oz. Label 001)

Label (Goyescas 7 Syrups Alcohol And Sugar Free 6 Oz. Label 001)
Drug Facts panel for Goyescas 7 Syrups Alcohol and Sugar Free Cough and Cold shows active ingredients: Dextromethorphan HBr 10 mg, Guaifenesin 100 mg, and Phenylephrine HCl 5 mg per 5 mL, with corresponding purposes as cough suppressant, expectorant, and nasal decongestant. It includes uses, warnings, directions for dosing by age group, and inactive ingredients list. The label features the product logo and labeler information for Goyescas of Fla.*

* 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.