Cetirizine Hydrochloride Tablet
Product Images NDC 65162-045

3 FDA label images from Amneal Pharmaceuticals Llc · 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 Cetirizine Hydrochloride (NDC 65162-045). 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

118c2ce0-figure-01 (118c2ce0 Figure 01)

118c2ce0-figure-01 (118c2ce0 Figure 01)
Cetirizine Hydrochloride 5 mg tablets packaging label by Amneal Pharmaceuticals LLC. The label indicates the product is an oral antihistamine tablet for allergy relief, containing 30 tablets. The label includes Drug Facts such as active ingredient, uses, warnings, and asks patients to see a doctor before use if needed. The packaging displays the NDC 65162-045-03, barcode, and instructions not to use if the imprinted foil inner seal is broken.*
FDA Label Image

118c2ce0-figure-02 (118c2ce0 Figure 02)

118c2ce0-figure-02 (118c2ce0 Figure 02)
Drug Facts panel for Cetirizine Hydrochloride 5 mg oral tablets by Amneal Pharmaceuticals LLC. The panel provides warnings including allergy alert, usage instructions, breastfeeding precautions, storage instructions, directions for dosage based on age, overdose information, inactive ingredients, and a contact number for questions or comments.*
FDA Label Image

118c2ce0-figure-03 (118c2ce0 Figure 03)

118c2ce0-figure-03 (118c2ce0 Figure 03)
Cetirizine Hydrochloride 5 mg tablets packaging label from Amneal Pharmaceuticals LLC. The label indicates the product is an allergy relief oral tablet containing 5 mg of cetirizine. The foldout carton design includes drug facts, active ingredients, warnings, use directions, inactive ingredients, and contact information for questions or comments. The National Drug Code (NDC) 65162-045-03 is shown with a barcode on the label.*

* 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.