Phenylephrine Hydrochloride Injection
Product Images NDC 31722-344

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Phenylephrine Hydrochloride (NDC 31722-344). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber Pharmaceuticals, 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
FDA Label Image

Phenylephrinehcl100mg1scartonlabel (Phenylephrinehcl100mg1scartonlabel)

Phenylephrinehcl100mg1scartonlabel (Phenylephrinehcl100mg1scartonlabel)
Packaging label for Phenylephrine Hydrochloride Injection, USP 10 mg/mL (100 mg/10 mL) intravenous injection, supplied in a 10 mL vial. Label highlights that the product must be diluted before intravenous use and protects from light. Manufactured by Aspiro Pharma Limited, distributed by Camber Pharmaceuticals, Inc. The label notes it as a pharmacy bulk package, not for direct infusion, with storage instructions and ingredient details.*
FDA Label Image

Phenylephrinehcl100mgcontainerlabel (Phenylephrinehcl100mgcontainerlabel)

Phenylephrinehcl100mgcontainerlabel (Phenylephrinehcl100mgcontainerlabel)
Label for Phenylephrine Hydrochloride Injection, USP 10 mg/mL (100 mg/10 mL) vial by Camber Pharmaceuticals, Inc. The label states it is for intravenous use, must be diluted, and includes handling and storage instructions. It is a 10 mL pharmacy bulk vial, not for direct infusion, manufactured by Aspiro Pharma Limited, India.*
FDA Label Image

Phenylephrinehcl10mg10scartoblabel (Phenylephrinehcl10mg10scartoblabel)

Phenylephrinehcl10mg10scartoblabel (Phenylephrinehcl10mg10scartoblabel)
Packaging label for Phenylephrine Hydrochloride Injection, USP 10 mg/mL by Camber Pharmaceuticals, Inc. The label indicates the product is for intravenous use and must be diluted. It contains 10 x 1 mL single-dose vials and instructs to discard unused portion. Additional storage and usage instructions are provided, along with manufacturer and barcode information.*
FDA Label Image

Phenylephrinehcl10mgcontainerlabel (Phenylephrinehcl10mgcontainerlabel)

Phenylephrinehcl10mgcontainerlabel (Phenylephrinehcl10mgcontainerlabel)
Label for Phenylephrine Hydrochloride Injection, USP 10 mg/mL for intravenous use. The label indicates a 1 mL single-dose vial, manufactured for Camber Pharmaceuticals, Inc., with manufacturing license number and barcodes visible. The product is Rx only and must be diluted before use. The manufacturer is listed as Aspiro Pharma Ltd, India.*
FDA Label Image

Phenylephrinehcl50mg10scartonlabel (Phenylephrinehcl50mg10scartonlabel)

Phenylephrinehcl50mg10scartonlabel (Phenylephrinehcl50mg10scartonlabel)
Box label for Phenylephrine Hydrochloride Injection, USP 50 mg/5 mL (10 mg/mL) for intravenous use by Camber Pharmaceuticals, Inc. The label states the product is Rx only, must be diluted, and protected from light. It contains 10 vials of 5 mL each. Manufacturer details include Camber Pharmaceuticals, Inc. in Piscataway, NJ, and Aspro Pharma Limited in India. The label warns it is a pharmacy bulk package not for direct infusion.*
FDA Label Image

Phenylephrinehcl50mgcontainerlabel (Phenylephrinehcl50mgcontainerlabel)

Phenylephrinehcl50mgcontainerlabel (Phenylephrinehcl50mgcontainerlabel)
Label for Phenylephrine Hydrochloride Injection, USP 50 mg/5 mL (10 mg/mL) in a 5 mL vial. It is indicated for intravenous use and must be diluted. The label notes this is a pharmacy bulk package, not for direct infusion, with storage instructions and manufacturer details for Camber Pharmaceuticals, Inc. and Aspiro Pharma Limited.*

* 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.