Xylocaine
Product Images NDC 21695-466

3 FDA label images from Rebel Distributors Corp · 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 Xylocaine (NDC 21695-466). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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

Lidocaine Chemical Structure (57964c72 5ffe 4548 Bca0 A5b0ca57ecb1 01)

Lidocaine Chemical Structure (57964c72 5ffe 4548 Bca0 A5b0ca57ecb1 01)
Chemical structure of the active ingredient in XYLOCAINE by Rebel Distributors Corp, showing a substituted aromatic ring connected to an amide and an amine group with associated hydrochloride (HCl).*
FDA Label Image

Epinephrine Chemical Structure (57964c72 5ffe 4548 Bca0 A5b0ca57ecb1 02)

Epinephrine Chemical Structure (57964c72 5ffe 4548 Bca0 A5b0ca57ecb1 02)
Chemical structure diagram of the active ingredient in XYLOCAINE by Rebel Distributors Corp, showing a benzene ring substituted with hydroxyl groups and an aminomethyl group with associated stereochemistry.*
FDA Label Image

Xylocaine 1% (57964c72 5ffe 4548 Bca0 A5b0ca57ecb1 03)

Xylocaine 1% (57964c72 5ffe 4548 Bca0 A5b0ca57ecb1 03)
The label for Xylocaine 1% 20ml vial by Rebel Distributors Corp shows the proprietary name, drug concentration, and volume. It lists active ingredients lidocaine HCl 10 mg, sodium chloride 7 mg, and methylparaben 1 mg per milliliter. The label includes the NDC number 21695-466-20 and states the product is RX only, distributed by Physician Partner in Thousand Oaks, CA. Storage instructions and safety warnings are printed at the bottom.*

* 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.