Cetirizine Hydrochloride (allergy) Capsule
Product Images NDC 58602-806

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 58602-806). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth 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.

Product Images & Figures Index

FDA Label Image

Package Label-principal Display Panel (10 mg (12's Capsule Container Carton Label))

Package Label-principal Display Panel (10 mg (12's Capsule Container Carton Label))
The image shows the base label and booklet pages for Cetirizine Hydrochloride Capsules 10 mg by Aurohealth LLC. The base label highlights the product name, strength, and form as liquid-filled capsules, with a package size of 12 capsules. It includes a tamper-evident seal warning and distributor information. The booklet contains extended Drug Facts covering uses, warnings, directions, inactive ingredients, and contact information.*
FDA Label Image

Package Label-principal Display Panel -10 mg (carton Label) (Cetirizine Allergy Fig2)

Package Label-principal Display Panel -10 mg (carton Label) (Cetirizine Allergy Fig2)
Packaging label for Cetirizine Hydrochloride Capsules 10 mg by Aurohealth LLC. The green and yellow label indicates the product is an oral antihistamine for allergy relief, containing 12 liquid gel capsules per package. The label includes Drug Facts panels with active ingredient, uses, warnings, directions, and storage information. The label also has barcodes and lot/expiration date areas.*

* 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.