Zodryl Dec 60
Product Images NDC 43378-125

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zodryl Dec 60 (NDC 43378-125). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Codadose, Inc., 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

980d54c0-figure-01 (980d54c0 Figure 01)

Label for Zodryl DEC 60 oral liquid, containing pseudoephedrine HCl as a decongestant, guaifenesin as an expectorant, and codeine phosphate as a cough suppressant. The label includes the NDC 43378-125-08, dosage form as an 8 FL OZ (236 mL) bottle, and instructions to shake well. The labeler is CodaDose, Inc.*

FDA Label Image

980d54c0-figure-02 (980d54c0 Figure 02)

Drug Facts panel for Zodryl DEC 60 by CodaDose, Inc. The panel lists active ingredients with their purposes: Codeine phosphate 1 mg as cough suppressant, Guaifenesin 20 mg as expectorant, and Pseudoephedrine HCl 4 mg as decongestant. It includes uses for temporary relief of symptoms related to minor throat and bronchial irritation and cold symptoms. The inactive ingredients section names components like bittermask, citric acid, FD&C colorants, flavors, sweeteners, and preservatives. Contact information and patent notices are also present.*

FDA Label Image

980d54c0-figure-03 (980d54c0 Figure 03)

Drug Facts label panels for Zodryl DEC 60 include warnings about use in children with certain conditions, instructions to consult a doctor or pharmacist before use, recommended dosage limits, directions for use, and storage information. The label emphasizes keeping the product out of children's reach and seeking professional help in case of overdose or serious symptoms.*

* 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.