Na
Product Images NDC 83090-007

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 Na (NDC 83090-007). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sintetica Us 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

The Image Of Ampoule Label (Ampoulelabel)

The Image Of Ampoule Label (Ampoulelabel)
Label for Lidocaine Hydrochloride Injection USP 4% (40 mg/mL), 200 mg/5 mL single dose ampule from Sintetica S.A. The label states it is preservative-free, for topical use and retrobulbar injection only, and indicates discard of unused portion. Manufactured in Switzerland.*
FDA Label Image

Lidocainehydrochloride (Lidocainehydrochloride)

Lidocainehydrochloride (Lidocainehydrochloride)
Chemical structure representing a compound containing a dimethyl-substituted benzene ring attached to an amide linked to a diethyl-substituted amine, associated with hydrochloride and water molecules, as shown in the formula. The labeler is Sintetica US LLC with Product NDC 83090-007.*
FDA Label Image

The Image Of The Carton (Outercarton)

The Image Of The Carton (Outercarton)
Lidocaine Hydrochloride Injection, USP 4% (200 mg/5 mL, 40 mg/mL) label from Sintetica US LLC. The single-dose ampule packaging contains 10 x 5 mL bottles and is preservative free. The label notes the product is for topical use and retrobulbar injection only, sterile and non-pyrogenic, and includes storage instructions and safety warnings.*

* 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.