Alcaftadine Solution/ Drops
Product Images NDC 68083-649

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Alcaftadine (NDC 68083-649). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma Limited, 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

Alcaftadine-spl-carton-label-mono-pack (Alcaftadine Spl Carton Label Mono Pack)

Packaging label for Alcaftadine Ophthalmic Solution 0.25%, an antihistamine eye drop by Gland Pharma Limited. The label states it is a 3 mL bottle providing once daily relief from eye allergy itch with a 40-day supply. The solution is indicated for ages 2 and older and provides relief from allergens such as pet dander, pollen, grass, and ragweed. It is sterile and for external ophthalmic use only.*

FDA Label Image

Alcaftadine-spl-carton-label-twin-pack (Alcaftadine Spl Carton Label Twin Pack)

Alcaftadine Ophthalmic Solution 0.25% antiasthmatic eye drops in a twin pack containing two 3 mL bottles (0.10 fl oz each) for once daily relief of eye allergy itch. The packaging highlights relief from pet dander, pollen, grass, and ragweed allergens, providing an 80 day supply. It is labeled sterile and manufactured by Gland Pharma Limited.*

FDA Label Image

Alcaftadine-spl-container-label (Alcaftadine Spl Container Label)

Label for Alcaftadine Ophthalmic Solution 0.25% (2.5 mg/mL), a sterile antihistamine eye drops solution in a 0.10 fl oz (3 mL) bottle. Manufactured by Gland Pharma Limited, Hyderabad, India. The label includes storage instructions (15° to 25°C), tamper-evident warnings, and space for lot and expiration dates.*

* 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.