Cetirizine Hydrochloride (allergy) Tablet
Product Images NDC 0363-9602

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 Cetirizine Hydrochloride (allergy) (NDC 0363-9602). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Walgreen Co., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Package Label-principal Display Panel (10 mg (30 Tablets Container Label))

Package Label-principal Display Panel (10 mg (30 Tablets Container Label))
Label for Walgreens Allergy Relief 10 mg Cetirizine Hydrochloride tablets, 30 count. The label states it is a 24-hour allergy relief antihistamine at original prescription strength. It includes active ingredient information, usage directions, warnings, storage instructions, and manufacturing details by Walgreen Co. The NDC number is 0363-9602-09.*
FDA Label Image

Package Label-principal Display Panel (10 mg (30 Tablets Container carton Label))

Package Label-principal Display Panel (10 mg (30 Tablets Container carton Label))
Cetirizine Hydrochloride (Allergy) Allergy Relief 10 mg oral tablets by Walgreen Co. The green carton features 'Allergy Relief' prominently, indicating 24-hour allergy relief with cetirizine hydrochloride USP 10 mg as the active ingredient. The package contains 30 tablets and highlights relief for indoor and outdoor allergies. Additional panels display drug facts, warnings, usage directions, and manufacturer information. The label includes a barcode and a sample image of the bottle inside.*

* 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.