Bimatoprost Solution/ Drops
Product Images NDC 0781-6206

4 FDA label images from Sandoz Inc · 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 Bimatoprost (NDC 0781-6206). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sandoz 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 Chemical Structure (Image 01)

Bimatoprost Chemical Structure (Image 01)
Chemical structure diagram of Bimatoprost, showing the molecular formula including hydroxyl groups, an ethyl chain, and a phenyl group consistent with the active pharmaceutical ingredient Bimatoprost.*
FDA Label Image

Illustration 1 (Image 02)

Illustration 1 (Image 02)
An instructional illustration showing a person dispensing a drop from a dropper bottle onto the tip of an applicator brush, likely demonstrating how to apply ophthalmic solution drops.*
FDA Label Image

Illustration 2 (Image 03)

Illustration 2 (Image 03)
An instructional black and white illustration showing the application of ophthalmic solution to the upper eyelid margin of a closed eye using a dropper. The image emphasizes precise medication administration near the eyelashes.*
FDA Label Image

Carton (Image 04)

Carton (Image 04)
Packaging label for Bimatoprost Ophthalmic Solution 0.03%, a 3 mL sterile solution/drops for topical application to the upper eyelid. The product is prescription-only and labeled with the NDC 0781-6206-93. It is manufactured by Sandoz Inc, a Novartis division, with references to product origin and storage instructions included on the label.*

* 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.