Latisse 01
Chemical structure diagram of bimatoprost, the active ingredient in LATISSE ophthalmic solution 0.3 mg/mL by Allergan, Inc.*
Latisse Solution/ Drops
Product Images NDC 0023-3616
6 FDA label images from Allergan, Inc. · Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Latisse (NDC 0023-3616). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Allergan, 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.
Product Images & Figures Index
Latisse 02
Latisse 03
The image shows the packaging label for LATISSE 0.3 mg/mL ophthalmic solution/drops. The label prominently displays the product name LATISSE and the active ingredient bimatoprost. The labeler is Allergan, Inc., and the product NDC is 0023-3616. The design includes dosage form and route information.*
Latisse 04
An instructional image showing the proper use of LATISSE ophthalmic solution 0.3 mg/mL. It depicts a person holding an applicator brush and applying a drop of the solution from the LATISSE bottle onto the brush tip for eyelash treatment.*
Latisse 05
An illustration showing the application of LATISSE ophthalmic solution to the upper eyelid using a thin brush or applicator. The image demonstrates proper technique for applying the solution near the base of the eyelashes.*
Latisse 06
Packaging label for LATISSE ophthalmic solution 0.03%, containing the active ingredient bimatoprost. The label displays product information including strength, dosage form (solution/drops), and usage instructions. It is labeled for prescription use and produced by Allergan, Inc. The label includes branding, regulatory text, and a barcode.*
* 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.
