Light Zinc Injection (Zinc Sulfate Heptahydrate)
Zinc Sulfate Hydrate 4.4mg
Injections · Prescription medication
Light Pharmtech Co., Ltd.
MFDS item code 202004671 · Notified 2020.06.26
This product's status changed to Expired on 2025.06.26. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Prevention of zinc deficiency and improvement of nutritional status
Patients receiving total parenteral nutrition (TPN) are prone to zinc deficiency, thus zinc supplementation is necessary. Zinc is an important mineral that enhances immune function and aids wound healing. Therefore, proper zinc supplementation during TPN can improve nutritional status and prevent complications.
Metabolically stable TPN patients: 2.5 to 4 mg/day Adult patients with fluid loss from the small intestine: an additional 12.2 mg/L (amount of fluid loss) or an additional 17.1 mg/kg (amount of excretion) Acute burn status: 4.5 to 6 mg/day To be used according to a doctor's prescription while monitoring plasma trace mineral levels for dosage adjustment.
Children under 5 years: 100 ug/kg/day For infants weighing less than 3 kg: 300 ug/kg/day
This drug should not be injected directly into peripheral veins without dilution. This is because administering in this manner can cause venous inflammation or increase the loss of zinc through the kidneys. The amount of zinc contained in this drug is very small, so toxic symptoms rarely appear. When mixing this drug with TPN (total parenteral nutrition) solution, it is advisable to prepare it in a special environment to maintain sterility. Additionally, before injection, the solution must be visually checked for any precipitate or discoloration. When administering zinc, using it together with copper may reduce the concentration of copper in the blood, so the concentrations of both components should be tested at regular intervals as a reference for dosing. This drug is excreted from the body through the intestines and kidneys, so patients with impaired excretory function should be careful as zinc may accumulate in the body. When administering this drug to pregnant or breastfeeding women, it should only be used if the benefits of treatment outweigh the risks, as its safety has not been fully confirmed. Zinc can pass through the placenta and may be present in breast milk. If zinc is overdosed, severe symptoms such as nausea, vomiting, dehydration, electrolyte imbalance, dizziness, abdominal pain, drowsiness, and ataxia may occur, so caution is advised. This drug should be stored out of the reach of children and kept in its original packaging in a dry place at room temperature. As it does not contain preservatives, any unused portions must be discarded.
Not everyone experiences these, and they can vary from person to person.
This drug must be stored in a sealed container to prevent air and moisture from entering, and the storage temperature should be maintained between 1 and 30 degrees Celsius. This will help maintain the drug's efficacy and safety.
A colorless, odorless, transparent liquid in a colorless, transparent vial injection.
10 milliliters/vial
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.