Phenylephrine Hydrochloride Injection
Product Images NDC 70069-801

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Phenylephrine Hydrochloride (NDC 70069-801). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, Llc, 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

1ml Side1 (1 mL Side1)

Packaging label for Phenylephrine HCl Injection USP 10 mg/mL by Somerset Therapeutics, LLC. The label indicates a 25 x 1 mL single-dose vial pack, listing ingredients including phenylephrine hydrochloride 10 mg per mL and other components, with storage instructions and manufacturing details noting production by Caplin Steriles Limited, India.*

FDA Label Image

10ml Carton (10ml Carton)

Label for Phenylephrine HCl Injection, USP 100 mg/10 mL (10 mg/mL) by Somerset Therapeutics, LLC. The label indicates a 10 mL vial for intravenous use, highlighting it as a pharmacy bulk package that must be diluted and is not for direct infusion. Storage and manufacturer details, ingredient list, and usage instructions are included.*

FDA Label Image

Image7 (10ml Vial Label)

Label for Phenylephrine HCl Injection USP 100 mg/10 mL (10 mg/mL) by Somerset Therapeutics, LLC. This pharmacy bulk package is indicated for intravenous use and must be diluted prior to use. The 10 mL vial is labeled for pharmacy bulk use only and not for direct infusion, with storage instructions and usage guidelines detailed on the label.*

FDA Label Image

Image1 (1ml Vial Label)

Label for Phenylephrine HCl Injection, USP 10 mg/mL in a 1 mL single-dose vial for intravenous use. The label includes a barcode, NDC 70069-801-01, and states the product is Rx only. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL, and made in India. Instructions note the solution must be diluted and unused portions discarded.*

FDA Label Image

Side2 1ml (2 1 mL Side)

Packaging label for Phenylephrine HCl Injection, USP 10 mg/mL intravenous injection by Somerset Therapeutics LLC. The label indicates single-dose vials of 1 mL, 25 vials per carton. It includes instructions to dilute before use, discard unused portions, store in carton until use, and protect from light. The label also notes vial stoppers do not contain natural rubber latex.*

FDA Label Image

5ml Side2 (2 5 mL Side)

Label for Phenylephrine HCl Injection, USP 50 mg/5 mL (10 mg/mL) intravenous injection by Somerset Therapeutics LLC. Package contains 10 vials of 5 mL multiple-dose vials intended for pharmacy bulk use and must be diluted before administration. Label includes storage instructions to protect from light and notes the vial stoppers are not made with natural rubber latex.*

FDA Label Image

Side1 5ml (5 mL Side1)

Unfolded packaging label for Phenylephrine Hydrochloride injection, 10 mg/mL. The label lists inactive ingredients like sodium chloride and citric acid, storage instructions 20°C to 25°C, and instructs to see the package insert for directions. Manufactured for Somerset Therapeutics, LLC, Hollywood, FL, and made by Caplin Steriles Limited, India.*

FDA Label Image

Image4 (5ml Vial Label)

Label for Phenylephrine HCl Injection, USP, 50 mg/5 mL (10 mg/mL) for intravenous use. The Pharmacy Bulk Package is marked as not for direct infusion and must be diluted. It contains a 5 mL vial and is manufactured for Somerset Therapeutics, LLC. The label includes storage, usage, and handling instructions.*

FDA Label Image

Image1 (Phenylephrine 1)

Chemical structure of phenylephrine hydrochloride, showing the molecular arrangement of atoms including a benzene ring with hydroxyl groups, and an amine functional group attached to a side chain.*

* 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.