Cetirizine Hydrochloride Tablet
Product Images NDC 65162-046

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cetirizine Hydrochloride (NDC 65162-046). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Llc, 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

4061bbde-figure-01 (4061bbde Figure 01)

Cetirizine Hydrochloride 10 mg tablets packaging label from Amneal Pharmaceuticals LLC. The label indicates an oral antihistamine allergy medication with a count of 30 tablets. It features the product's NDC 65162-046-03 and includes sections for Drug Facts such as active ingredient, uses, and warnings.*

FDA Label Image

4061bbde-figure-02 (4061bbde Figure 02)

Drug Facts panel continuation for Cetirizine Hydrochloride 10 mg oral tablet by Amneal Pharmaceuticals LLC. Contains warnings for adults, directions for use, storage instructions, inactive ingredients, and contact information for questions or comments. Notable details include age-specific dosing instructions and storage at room temperature away from moisture and heat.*

FDA Label Image

4061bbde-figure-03 (4061bbde Figure 03)

The image shows a carton packaging label for Cetirizine Hydrochloride Tablets, 10 mg, manufactured by Amneal Pharmaceuticals LLC. The label states the product contains 30 tablets and highlights it as an antihistamine allergy medication. The label includes Drug Facts information, warnings, active ingredients, dosage directions, and storage instructions.*

* 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.