Zodryl Ac 25
Product Images NDC 43378-100

3 FDA label images from Codadose, Inc. · 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 Zodryl Ac 25 (NDC 43378-100). 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

07b96821-figure-01 (07b96821 Figure 01)

07b96821-figure-01 (07b96821 Figure 01)
Label for Zodryl AC 25, an oral liquid containing 25 mg strength of active ingredients chlorpheniramine maleate (antihistamine) and codeine phosphate (cough suppressant). The label indicates grape flavor and a 4 fl oz (118 mL) bottle size. It is labeled by CodaDose, Inc. and includes directions to shake well along with warnings about sedatives or tranquilizers.*
FDA Label Image

07b96821-figure-02 (07b96821 Figure 02)

07b96821-figure-02 (07b96821 Figure 02)
The image shows the front panel and a back panel layout for Zodryl AC 25, a pharmaceutical product by CodaDose, Inc. The front (cover) panel includes a barcode and drug facts with active ingredients and uses. The back panel contains additional drug facts with inactive ingredients, question contact information, and manufacturer details. Dimensions for each panel are marked.*
FDA Label Image

07b96821-figure-03 (07b96821 Figure 03)

07b96821-figure-03 (07b96821 Figure 03)
Drug Facts panels from the back cover of Zodryl AC 25 packaging, including warnings, information on acetaminophen use as a fever reducer and pain reliever, aspirin precautions, and directions for use. The panels provide safety instructions, dosage directions, and storage recommendations.*

* 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.