Zodryl Ac 40
Product Images NDC 43378-103

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 40 (NDC 43378-103). 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.

Product Images & Figures Index

FDA Label Image

Acbdfd6d-figure-01 (Acbdfd6d Figure 01)

Acbdfd6d-figure-01 (Acbdfd6d Figure 01)
Label for Zodryl AC 40 oral liquid by CodaDose, Inc., containing chlorpheniramine maleate (antihistamine) and codeine phosphate (cough suppressant). The grape-flavored 4 FL OZ (118 mL) bottle includes instructions to shake well and warnings against use with sedatives or tranquilizers. The label features the NDC 43378-103-04 and dosage details.*
FDA Label Image

Acbdfd6d-figure-02 (Acbdfd6d Figure 02)

Acbdfd6d-figure-02 (Acbdfd6d Figure 02)
Label for Zodryl AC 40 by CodaDose, Inc., showing Drug Facts with active and inactive ingredients sections. The label includes a barcode, measurements for label dimensions, and usage instructions. It is a rectangular front label with sections for drug facts and manufacturer information.*
FDA Label Image

Acbdfd6d-figure-03 (Acbdfd6d Figure 03)

Acbdfd6d-figure-03 (Acbdfd6d Figure 03)
Drug Facts panel of Zodryl AC 40 showing warnings, directions, and dosing information. The text includes instructions for safe use, potential side effects, and age restrictions, as well as storage recommendations, segmented across two pages labeled as Page #2 (Back of Cover) and Page #3.*

* 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.