Zinc Sulfate Injection, Solution
Product Images NDC 31722-455

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Zinc Sulfate (NDC 31722-455). 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
FDA Label Image

Zincsulfateinjection10mgcartonlabel (Zincsulfateinjection10mgcartonlabel)

Zincsulfateinjection10mgcartonlabel (Zincsulfateinjection10mgcartonlabel)
Zinc Sulfate Injection, USP 10 mg/10 mL (1 mg/mL) of zinc injection solution for intravenous use after dilution and admixing. The packaging label indicates a pharmacy bulk package of 25 x 10 mL sterile vials, labeled for prescription use only and not for direct infusion. Labeler is Camber Pharmaceuticals, Inc., with additional manufacturing information from Aspiro Pharma Limited.*
FDA Label Image

Zincsulfateinjection10mgcontainerlabel (Zincsulfateinjection10mgcontainerlabel)

Zincsulfateinjection10mgcontainerlabel (Zincsulfateinjection10mgcontainerlabel)
Label for Zinc Sulfate Injection, USP 10 mg/10 mL (1 mg/mL) solution for intravenous use after dilution and admixing. Pharmacy bulk package, sterile, 10 mL vial. Manufactured by ASPIRO PHARMA LIMITED, India, with storage and usage instructions included.*
FDA Label Image

Zincsulfateinjection25mgcartonlabel (Zincsulfateinjection25mgcartonlabel)

Zincsulfateinjection25mgcartonlabel (Zincsulfateinjection25mgcartonlabel)
Packaging label for Zinc Sulfate Injection, USP 25 mg*/5 mL (5 mg/mL) sterile intravenous solution, supplied as 25 x 10 mL vials. The label indicates it is for intravenous use after dilution and admixing, marked as a pharmacy bulk package not for direct infusion. Manufactured by Aspiro Pharma Limited, with storage and usage instructions included.*
FDA Label Image

Zincsulfateinjection25mgcontainerlabel (Zincsulfateinjection25mgcontainerlabel)

Zincsulfateinjection25mgcontainerlabel (Zincsulfateinjection25mgcontainerlabel)
Zinc Sulfate Injection, USP 25 mg/5 mL (5 mg/mL) intravenous solution for injection, labeled as pharmacy bulk package not for direct infusion. The sterile 5 mL vial is manufactured by Aspiro Pharma Limited, India, labeled for use after dilution and admixing, with storage instructions and contact information included.*
FDA Label Image

Zincsulfateinjection30mgcartonlabel (Zincsulfateinjection30mgcartonlabel)

Zincsulfateinjection30mgcartonlabel (Zincsulfateinjection30mgcartonlabel)
The image shows the carton label for Zinc Sulfate Injection, USP, 30 mg/10 mL (3 mg/mL) of zinc, for intravenous use. It is labeled as a pharmacy bulk package, not for direct infusion, containing 25 vials of 10 mL each. The label includes storage information, manufacturer Aspiro Pharma Limited, and a U.S. contact number.*
FDA Label Image

Zincsulfateinjection30mgcontainerlabel (Zincsulfateinjection30mgcontainerlabel)

Zincsulfateinjection30mgcontainerlabel (Zincsulfateinjection30mgcontainerlabel)
Label for Zinc Sulfate Injection, USP 30 mg per 10 mL (3 mg per mL) intravenous solution in a 10 mL pharmacy bulk package. The label states it is sterile and not for direct infusion, intended for intravenous use after dilution and admixing. It includes storage instructions and manufacturer details (Aspiro Pharma Limited, India).*
FDA Label Image

Zincsulfateinjectionstructure (Zincsulfateinjectionstructure)

Zincsulfateinjectionstructure (Zincsulfateinjectionstructure)
Chemical structure of zinc sulfate showing a central sulfate ion (SO4) surrounded by water molecules (H2O) and a zinc ion (Zn2+). The diagram depicts zinc sulfate hydrate with coordinated water molecules.*

* 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.