Na
Product Images NDC 68055-649

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 68055-649). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sintetica Sa, 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% (200 mg/5 mL) single dose ampule. The label indicates the product is preservative free and intended only for topical use and retrobulbar injection. Manufactured by Sintetica S.A., Switzerland, with a 5 mL volume. Includes lot and expiration date fields and the NDC 68055-649-01.*
FDA Label Image

Lidocainehydrochloride (Lidocainehydrochloride)

Lidocainehydrochloride (Lidocainehydrochloride)
Chemical structure diagram depicting a molecule labeled with groups including CH3, NHCOCH2N(C2H5)2, HCl, and H2O, indicating the chemical composition of the active ingredient associated with the SINTETICA SA product NDC 68055-649.*
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) single-dose ampules by Sintetica SA. The label indicates it is preservative-free and intended only for topical use and retrobulbar injection. The package contains 10 x 5 mL ampules and is sterile and non-pyrogenic. Storage instructions and dosage information are provided.*

* 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.