Eohilia Suspension
Product Images NDC 64764-105

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Eohilia (NDC 64764-105). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Takeda Pharmaceuticals America, 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

Chemical Structure (Eohilia 01)

Chemical structure of Budesonide shown with carbon rings, hydroxyl groups, and various bonds representing its molecular configuration.*

FDA Label Image

Figure A (Eohilia 02)

FDA Label Image

Figure B (Eohilia 03)

An instructional illustration showing a hand holding and shaking a bottle, indicating the medication should be shaken before use.*

FDA Label Image

Figure C (Eohilia 04)

An instructional illustration depicting a person swallowing an oral suspension medication from a container. The image shows the outline of a head with liquid being poured or administered into the mouth from a small bottle or cup.*

FDA Label Image

Figure D (Eohilia 05)

A black and white circular icon displaying the text "30 min" in the center, surrounded by clock tick marks suggesting a 30-minute time interval. This is likely an instructional or timing-related graphic.*

FDA Label Image

Principal Display Panel (10 mL Stick Pack Carton)

Packaging label for Eohilia (budesonide oral suspension) 2 mg/10 mL, an oral suspension by Takeda Pharmaceuticals America, Inc. The label indicates 60 single-dose 10 mL stick packs in a carton. The label includes directions to read enclosed instructions, ingredient information, and storage conditions. The product is cherry flavored.*

* 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.