Goprelto Solution
Product Images NDC 70839-359

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Goprelto (NDC 70839-359). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lxo Us 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

Carton (Carton)

Carton (Carton)
The packaging label for Goprelto (cocaine hydrochloride) nasal solution 160 mg/4 mL by LXO US Inc. This pharmaceutical carton label includes product identification, active ingredient concentration, usage instructions indicating it is for topical use only and not for injection or ophthalmic use, and storage conditions advising to avoid freezing and maintain specific temperatures. The label also displays manufacturer and distributor information along with barcodes and company logos.*
FDA Label Image

Label (Labels)

Label (Labels)
Goprelto 160 mg/4 mL cocaine hydrochloride nasal solution label from LXO US Inc. The label shows the NDC 70839-359-04, identifies it as a single-unit 4 mL solution for nasal use, with instructions stating it is for topical use only and not for injection or ophthalmic use. It includes inactive ingredients and storage instructions.*
FDA Label Image

Structure (Structure Goprelto Spl)

Structure (Structure Goprelto Spl)
Chemical structure diagram of cocaine hydrochloride showing the molecular arrangement of atoms and bonds, including a benzene ring and functional groups with a chloride ion (Cl-).*

* 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.