Chemical Structure (Zolymbus 01)
Zolymbus Gel
Product Images NDC 82584-010
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Zolymbus (NDC 82584-010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Thea Pharma 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.
Ifu Step 3 (Zolymbus 02)
Ifu Step 4 (Zolymbus 03)
Ifu Step 5-6-7 (Zolymbus 04)
Logo (Zolymbus 05)
Carton (Zolymbus 06)
ZOLYMBUS™ is a bimatoprost ophthalmic gel containing 0.01% bimatoprost. It is for topical ophthalmic use and comes in single-dose containers. The gel is designed for ophthalmic use and should only be used as directed. This product is prescription-only and contains active ingredient bimatoprost.*
Pouch (Zolymbus 07)
This is information regarding a medication with the NDC number 82584-010-81. The recommended dosage is to apply one drop in the affected eye(s) once daily in the evening from a single-dose container. Once opened, the foil pouch can be used for up to 14 days, then discard any unused containers after 14 days. The medication is ZOLYMBUS™, a bimatoprost ophthalmic gel with a concentration of 0.01%. It is for topical ophthalmic use and comes in 10 single-dose containers. The product does not contain preservatives and should be stored between 20-30°C.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
