Childrens Giltuss D Syrup
Product Images NDC 58552-148

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Childrens Giltuss D (NDC 58552-148). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gil Pharmaceutical 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

Image Description (Childrens Glituss Allery Congestion Bottle Label)

Image Description (Childrens Glituss Allery Congestion Bottle Label)
Label for Children's Giltuss-D Allergy & Congestion syrup, tutti frutti flavor, 4 fluid ounces (118 ml) by Gil Pharmaceutical Corp. This oral syrup is indicated for children ages 6 to 12 years to temporarily relieve symptoms related to allergies. The label includes active ingredients chlorpheniramine maleate 1.75 mg and phenylephrine HCl nasal decongestant, usage instructions, warnings, and storage information. The product is free from dye, preservatives, and sodium fluoride.*
FDA Label Image

Image Description (Childrens Glituss Allery Congestion Carton Label)

Image Description (Childrens Glituss Allery Congestion Carton Label)
Packaging label for Children's Giltuss-D Allergy & Congestion syrup, a human OTC drug by Gil Pharmaceutical Corp. The front panel shows the product name, indication for allergy and congestion relief, and a tutti frutti flavor. The active ingredients listed are Chlorpheniramine maleate 1.75 mg and Phenylephrine HCl 5 mg per 5 mL dose. The label includes warnings, directions, drug facts, and states it is dye-free, preservative-free, sodium-free, sugar-free, yeast-free, and gluten-free. The package size is 4 fl oz (118 mL).*

* 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.