Bimatoprost Solution/ Drops
Product Images NDC 62332-511

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Bimatoprost (NDC 62332-511). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic 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

Bimatoprost Bottle 3ml

Label for bimatoprost ophthalmic solution 0.03%, 3 mL solution/drops for topical application to the upper eyelid. Manufactured by Alembic Pharmaceuticals Inc. The label notes active ingredient strength as 0.3 mg/mL bimatoprost and contains benzalkonium chloride preservative. Includes storage instructions and space for lot and expiration dates.*

FDA Label Image

Bimatoprost-bottle-5ml (Bimatoprost Bottle 5ml)

Label for Bimatoprost Ophthalmic Solution 0.03%, containing 0.3 mg/mL bimatoprost, in a 5 mL bottle. The product is manufactured for Alembic Pharmaceuticals Inc., Bedminster, NJ, USA. The label includes storage instructions, active ingredient, preservative benzalkonium chloride 0.05 mg/mL, and NDC 62332-511-05.*

FDA Label Image

Bimatoprost Carton 3ml

Packaging label for Bimatoprost Ophthalmic Solution 0.03%, a prescription eye drop solution by Alembic Pharmaceuticals Inc. The carton indicates a 3 mL bottle of sterile solution with 70 disposable applicators for topical application to the upper eyelid. The label features dosage instructions, NDC 62332-511-03, and manufacturer information.*

FDA Label Image

Bimatoprost-carton-5ml (Bimatoprost Carton 5ml)

Packaging label for bimatoprost ophthalmic solution 0.03%, an ophthalmic solution by Alembic Pharmaceuticals Inc. The label indicates the product contains a 5 mL sterile solution bottle and 140 disposable applicators for topical application to the upper eyelid. The label shows NDC 62332-511-05 and includes storage instructions and ingredient details.*

FDA Label Image

Bimatoprost-illu1 (Bimatoprost Illu1)

An image showing a close-up of a white ophthalmic dropper bottle dispensing a drop of solution above a black angled brush held in a person's hand. The drop is poised at the tip of the dropper, illustrating the liquid form of an eye drop product.*

FDA Label Image

Bimatoprost-illu2 (Bimatoprost Illu2)

FDA Label Image

Bimatoprost-struc (Bimatoprost Struc)

Chemical structure diagram of bimatoprost, showing its molecular configuration with hydroxyl groups, a phenyl ring, and an ethanolamide moiety.*

* 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.