Alcaftadine Solution/ Drops
Product Images NDC 58602-605

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Alcaftadine (NDC 58602-605). 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.

FDA Label Image

Package Label-principal Display Panel-0.25 % (5 mL Container) (Alcaftadine Fig1)

Label for Alcaftadine Ophthalmic Solution 0.25%, an antihistamine eye drop solution. The sterile solution is supplied in a 0.17 fl oz (5 mL) bottle by Aurohealth LLC. The label includes storage instructions, tamper-evident warnings, and usage notes. The NDC number is 58602-605-40.*

FDA Label Image

Package Label-principal Display Panel-0.25% (10 mL Container Carton) (Alcaftadine Fig2)

Alcaftadine 0.25% Ophthalmic Solution, antihistamine eye drops in a 0.17 fl oz (5 mL) package by Aurohealth LLC. The label highlights use for eye allergy itch relief and once daily relief, with a 60 day supply indicated. The packaging includes Drug Facts with active ingredient, warnings, directions, inactive ingredients, and manufacturer details.*

FDA Label Image

Package Label-principal Display Panel-0.25% (5 mL Container Carton) Twin Pack (Alcaftadine Fig3)

Alcaftadine 0.25% ophthalmic solution packaging label from Aurohealth LLC. The original prescription strength eye drop solution is an antihistamine for allergy eye itch relief, offered as a twin pack with two 5 mL bottles. The label includes Drug Facts, usage, warnings, and storage instructions. The product claims once daily relief for eye allergies caused by pet dander, pollen, grass, and ragweed.*

* 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.