Levocetirizine Dihydrochloride Solution
Product Images NDC 31722-659

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Levocetirizine Dihydrochloride (NDC 31722-659). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber Pharmaceuticals, Inc., 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
FDA Label Image

Levocartonlabel (Levocartonlabel)

Levocartonlabel (Levocartonlabel)
Packaging label for Levocetirizine Dihydrochloride Oral Solution 2.5 mg/5 mL (0.5 mg/mL) by Camber Pharmaceuticals, Inc. The label indicates the product is a prescription oral solution in a 5 oz (148 mL) bottle. It includes storage instructions, dosage information referencing the package insert, contact number, and manufacturing details showing production by Hetero Labs Limited in India.*
FDA Label Image

Levocontlabel (Levocontlabel)

Levocontlabel (Levocontlabel)
Label for Levocetirizine Dihydrochloride Oral Solution 2.5 mg/5 mL (0.5 mg/mL) by Camber Pharmaceuticals, Inc. The label shows the product name, dosage form, strength, NDC number 31722-659-31, and volume 5 oz (148 mL). It includes storage instructions, a contact number, and manufacturing information indicating Hetero Labs in India. The label features barcodes and standard pharmaceutical warning and handling information.*
FDA Label Image

Levostructure (Levostructure)

Levostructure (Levostructure)
Chemical structure diagram of levocetirizine dihydrochloride, showing the molecular arrangement including aromatic rings, nitrogen atoms, and chloride groups, with .2HCl indicated as part of the structure.*

* 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.