Goniovisc
Product Images NDC 17238-610

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Goniovisc (NDC 17238-610). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hub Pharmaceuticals, Llc, 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

Goniovisc Bottle Label (Goniovisc Bottle Label)

Goniovisc Bottle Label (Goniovisc Bottle Label)
Drug Facts panel for Goniovisc Ophthalmic Lubricant containing Hypromellose USP 2.5% per mL as the active ingredient. The panel details usage as an eye lubricant, directions for instilling 1 or 2 drops as needed, storage instructions, inactive ingredients list, warnings, and manufacturer information for HUB Pharmaceuticals, LLC. It includes lot, expiration, and sterility indicators.*
FDA Label Image

Goniovisc Box Label (Goniovisc Box Label)

Goniovisc Box Label (Goniovisc Box Label)
Goniovisc Ophthalmic Lubricant Eye Lubricant Hypromellose Ophthalmic Solution, USP 2.5%, Drops (Sterile) 15 mL (1/2 fl. oz.) by HUB Pharmaceuticals, LLC. The label includes drug facts: active ingredient hypromellose USP 25 mg (2.5%) as lubricant, uses for relieving eye dryness, and warnings for external use only. Directions advise instilling 1 or 2 drops as needed. Contains inactive ingredients and preservative benzalkonium chloride NF 0.01% w/v. Manufactured by Contacare Ophthalmics and Diagnostics in India. Storage instructions specify 15°-30°C (59°-86°F), do not freeze. The label features the NDC 17238-610-15, barcode, and contact information.*

* 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.