Phenylephrine Hydrochloride Injection
Product Images NDC 0641-6229

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Phenylephrine Hydrochloride (NDC 0641-6229). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Structural Formula (Phenylephrine HCl Injection Usp Premierprorx 1)

Chemical structure of Phenylephrine Hydrochloride showing its molecular arrangement with hydroxyl, amine, and benzene ring components along with the hydrochloride moiety.*

FDA Label Image

462-786-00 (Phenylephrine HCl Injection Usp Premierprorx 2)

Label for Phenylephrine Hydrochloride Injection, USP 10 mg/mL single dose vial for intravenous use. Instructions state to dilute before use and protect from light. Manufactured by Hikma Pharmaceuticals USA Inc. Includes NDC 0641-6229 and barcode information.*

FDA Label Image

462-787-00 With Fix (Phenylephrine HCl Injection Usp Premierprorx 3)

Label for Phenylephrine Hydrochloride Injection, USP 10 mg/mL, for intravenous use. The product is provided in 25 single-dose 1 mL vials. The label instructs to dilute before use and to discard any unused portion. Manufactured by Hikma Pharmaceuticals USA Inc., Berkeley Heights, NJ. Storage and protective instructions are included.*

FDA Label Image

Layout 1 (Phenylephrine HCl Injection Usp Premierprorx 4)

Label panel showing a QR code alongside serialized text fields including GTIN, serial number (SN), expiration date (EXP), and lot number (LOT). This label is associated with Phenylephrine Hydrochloride injection 10 mg/mL from Hikma Pharmaceuticals USA Inc.*

* 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.