Donnatal Elixir
Product Images NDC 59212-422

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Donnatal (NDC 59212-422). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanz Pharma (us) Corp., 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

4oz-grape-bottle-label (4oz Grape Bottle Label)

This text provides important warnings and instructions for the medication Donnatal. It includes cautionary statements regarding the storage of the drug, overdose, and keeping it out of reach of children. The text also lists the ingredients and quantities for the medication, as well as prescribing and administrative information. The medication is distributed by Amdpharm Limited, and it is recommended to seek professional assistance or contact a Poison Control Center immediately in the event of an accidental overdose.*

FDA Label Image

4oz-mint-bottle-label (4oz Mint Bottle Label)

Donnatal is a prescription medication that contains Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide in mint flavor elixir form. It is recommended to keep the medicine out of reach of children and seek immediate professional help in case of an overdose. The medicine should be protected from heat and moisture and dispensed in a light-resistant container with an acid-resistant closure. Dosage instructions should be taken from the accompanying prescription information. The product is distributed by Amdipharm Limited and is manufactured in the United States.*

* 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.