Na
Product Images NDC 68055-645

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Na (NDC 68055-645). 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

Lidocainehydrochloride (Lidocaine Hydrochloride)

Chemical structure diagram illustrating the molecular composition of a compound associated with the labeler SINTETICA SA. The structure features a benzene ring substituted with two methyl groups, an amide linkage, an ethylamine side chain, and a hydrochloride component.*

FDA Label Image

Label Amp 1 10ml (Label Amp 1 10ml)

Packaging label for Lidocaine HCl Injection, USP 1% (10 mg/10 ml) by Sintetica SA. It specifies the product is for infiltration and nerve block including caudal and epidural use. The label notes the product contains no methylparaben, is for inhalation, and is a 10 mL single-dose ampul. Unused portions should be discarded.*

FDA Label Image

Label Amp 1 2ml (Label Amp 1 2ml)

Label for Lidocaine HCl Injection, USP 1% (20 mg/2 mL) manufactured by Sintetica SA. This 2 mL single-dose ampule is indicated for infiltration and nerve block including caudal and epidural use. The label notes it is methylparaben free and includes instructions to discard unused portions. Lot and expiration date fields are present but not filled.*

FDA Label Image

Label Amp 1 5ml (Label Amp 1 5ml)

Label for Lidocaine HCl Injection, USP 1% 50 mg/5 mL (10 mg/mL) manufactured by Sintetica SA. The label indicates it is for infiltration and nerve block including caudal and epidural use. It is methylparaben free, sterile, nonpyrogenic, and for prescription use only. The product is supplied in a 5 mL single-dose ampule.*

FDA Label Image

Label Amp 2 10ml (Label Amp 2 10ml)

Label for Lidocaine HCl Injection, USP 2% (20 mg/mL) 10 mL single-dose ampule. The label notes it is methylparaben free and not for inhalation. It is manufactured by Sintetica SA, located in Mendrisio, Switzerland. The label includes an NDC code 68055-647-01 and warnings for infiltration and nerve block use, with a section for lot and expiration data.*

FDA Label Image

Label Amp 2 2ml (Label Amp 2 2ml)

Label for Lidocaine HCl Injection, USP 2% (40 mg/mL) by Sintetica S.A. It is a 2 mL single-dose ampule intended for infiltration and nerve block, including caudal and epidural use. The product is methylparaben free. The label includes a barcode and spaces for lot and expiration date.*

FDA Label Image

Label Amp 2 5ml (Label Amp 2 5ml)

Label for Lidocaine HCl Injection, USP 2% (100 mg/5 mL) by Sintetica SA. It is a 20 mL single-dose ampule for infiltration and nerve block including caudal and epidural use. The label includes storage instructions, a warning about solution appearance, and Lot and Expiration date fields.*

FDA Label Image

Outer Carton 1 10ml (Outer Pack 1 10ml)

Label for Lidocaine Hydrochloride Injection, USP, 1% 100 mg/10 mL (10 mg/mL), manufactured by Sintetica SA, Switzerland. The label indicates the product is for infiltration and nerve block including caudal and epidural use, and is not for inhalation. It is methylparaben free and for prescription use only. The package contains 10 single-dose ampules of 10 mL each, with storage instructions and lot/expiration fields.*

FDA Label Image

Outer Carton 1 2ml (Outer Pack 1 2ml)

Lidocaine Hydrochloride Injection, USP 1% (20 mg/2 mL) vial label from Sintetica SA, Switzerland. The label indicates it is for infiltration and nerve block use, including caudal and epidural administration, methylparaben free. Each mL contains 10 mg lidocaine HCl and inactive ingredients. The package contains 10 x 2 mL single-dose ampules. Storage instructions and lot/expiration placeholders are shown.*

FDA Label Image

Outer Carton 1 5ml (Outer Pack 1 5ml)

Label for Lidocaine Hydrochloride Injection, USP 1% (50 mg/5 mL) by Sintetica S.A. The label indicates a strength of 10 mg/mL, intended for infiltration and nerve block including caudal and epidural use. The product is methylparaben free and for prescription use only. It is supplied in single-dose 5 mL ampules, with storage instructions and manufacturer details from Sintetica S.A., Switzerland.*

FDA Label Image

Outer Carton 2 10ml (Outer Pack 2 10ml)

Lidocaine Hydrochloride Injection, USP 2% 200 mg/10 mL (20 mg/mL) single-dose ampules for injection and nerve block, including caudal and epidural use. The label states the product is methylparaben-free, sterile, non-pyrogenic, and not for inhalation. Manufactured by Sintetica S.A., Switzerland, the package contains 10 x 10 mL ampules. It includes storage instructions and a barcode.*

FDA Label Image

Outer Carton 2 2ml (Outer Pack 2 2ml)

Lidocaine Hydrochloride Injection, USP 2% (40 mg/2 mL) vial label by Sintetica SA. Contains 20 mg/mL Lidocaine for infiltration and nerve block, including caudal and epidural use. The sterile, nonpyrogenic injection includes storage instructions, preservative information (methylparaben free), and manufacturer details in Switzerland. Single-dose ampules are indicated with usage and disposal directions.*

FDA Label Image

Outer Carton 2 5ml (Outer Pack 2 5ml)

Label for Lidocaine Hydrochloride Injection USP 2% (100 mg/5 mL) by Sintetica S.A., Switzerland. The label indicates use for infiltration and nerve block, including caudal and epidural use, and states it is methylparaben free. The package contains 10 single-dose 5 mL vials. Additional handling and storage instructions 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.