Phenylephrine Hydrochloride Injection
Product Images NDC 36000-358

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Phenylephrine Hydrochloride (NDC 36000-358). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Description (Image 01)

Chemical structure of phenylephrine hydrochloride depicting its molecular arrangement including hydroxyl groups, an amine group with a methyl substitution, and the associated hydrochloride (HCl) moiety.*

FDA Label Image

Image-02 (Image 02)

Label for phenylephrine hydrochloride injection, USP 10 mg/mL. The label indicates it is for intravenous use, must be diluted, and is a 1 mL single-dose vial. It is manufactured for Baxter Healthcare Corporation, Deerfield, IL, USA, and made in India. Storage instructions specify 20°C to 25°C with permitted excursions.*

FDA Label Image

Image-03 (Image 03)

Packaging label for Phenylephrine Hydrochloride Injection, USP 10 mg/mL by Baxter Healthcare Corporation. The label indicates it is for intravenous use, must be diluted, with instructions to discard unused portion. The package contains 25 single-dose vials of 1 mL each and advises to protect from light and store in the carton until use.*

FDA Label Image

Image-04 (Image 04)

Packaging label for Phenylephrine Hydrochloride Injection USP 10 mg/mL, an intravenous injection by Baxter Healthcare Corporation. The label includes dosage strength, storage instructions, manufacturer details, barcode, and notes such as vial stopper composition and dilution requirement for intravenous use.*

FDA Label Image

Image-05 (Image 05)

Label for Phenylephrine Hydrochloride Injection, USP 50 mg/5 mL (10 mg/mL) for intravenous use in a pharmacy bulk package. The 5 mL vial, must be diluted, and is not for direct infusion. Manufactured by Baxter Healthcare Corporation, with storage instructions and barcodes visible.*

FDA Label Image

Image-06 (Image 06)

Packaging label for Phenylephrine Hydrochloride Injection, USP 50 mg/5 mL (10 mg/mL) intravenous injection by Baxter Healthcare Corporation. The label indicates it is a pharmacy bulk package containing ten 5 mL vials, with instructions that it must be diluted and is not for direct infusion. Storage recommendations include protecting from light and storing in the carton until use.*

FDA Label Image

Image-07 (Image 07)

Packaging label for phenylephrine hydrochloride injection, 10 mg/mL, manufactured by Baxter Pharmaceuticals India Private Ltd and labeled for Baxter Healthcare Corporation. The label includes storage instructions, ingredient details, manufacturer information, and a barcode, intended for intravenous use.*

FDA Label Image

Image-08 (Image 08)

Label for Phenylephrine Hydrochloride Injection, USP, 100 mg/10 mL (10 mg/mL) bulk vial for intravenous use. The label indicates it is a pharmacy bulk package not for direct infusion, must be diluted, and protected from light. Manufactured for Baxter Healthcare Corporation, the label includes storage instructions and a barcode.*

FDA Label Image

Image-10 (Image 09)

Packaging label for Phenylephrine Hydrochloride Injection, USP 100 mg/10 mL (10 mg/mL) intravenous injection. This pharmacy bulk package contains 5 x 10 mL vials and is marked "Not for Direct Infusion" and must be diluted before use. Labeler is Baxter Healthcare Corporation. Storage instructions include protecting from light and storing in carton until use.*

FDA Label Image

Image-10.jpg (Image 10)

Phenylephrine Hydrochloride Injection, USP 10 mg/mL (100 mg/10 mL) vial label. The label includes manufacturer information—Baxter Pharmaceuticals India Private Ltd—and labeler, Baxter Healthcare Corporation. It states the product is for intravenous use, pharmacy bulk package (not for direct infusion), and must be diluted before administration. The label features storage instructions and a barcode.*

* 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.