Medication info
Powerking Soft Capsule

Powerking Soft Capsule

OTC medicationSoft capsule경구
Ingredient · strength
Cholecalciferol Concentrate Oil›0.4mg / 1 capsuleAscorbic Acid›75mg / 1 capsuleThiamine Hydrochloride›2mg / 1 capsuleRiboflavin›3mg / 1 capsuleNicotinamide›20mg / 1 capsuleRetinol Palmitate Oil›5mg / 1 capsule
Manufacturer / importer
(주)바스칸바이오제약
Appearance
Dark green oblong soft capsule containing yellowish-brown contents
Packaging
1 capsule/pack, 600 capsules/box [(1 capsule/pack x 600)]
Approval status
Active

MFDS item code 201702265 · Notified 2017.05.01

Summary

Main use
Improvement of physical fatigue and physical strength during pregnancy and breastfeeding, alleviation of eye dryness, prevention of bone development deficiency due to vitamin supplementation.
Who takes it
Adults
Adult dose
For adults: 1 capsule once a day

Ingredients

Manufacturer
(주)바스칸바이오제약

Efficacy & effects

Improvement of physical fatigue and physical strength during pregnancy and breastfeeding, alleviation of eye dryness, prevention of bone development deficiency due to vitamin supplementation.

  • Physical fatigue
  • decreased physical strength
  • dry eyes
  • night blindness
  • poor bone development
  • poor tooth development
View approved original text

This drug provides vitamins A, D, B1, B2, and C to individuals experiencing physical fatigue or those with decreased physical strength during pregnancy, breastfeeding, illness, or post-illness, as well as children in their growth period and the elderly. It also alleviates eye dryness and improves night blindness, and helps with poor bone and tooth development. It is effective in preventing rickets, supporting healthy growth and recovery. This drug is used to enhance overall physical strength, eye health, and bone development.

How to take

Adult dose

For adults: 1 capsule once a day

Precautions

This drug should not be taken in doses exceeding 5,000 IU per day by women in the first three months of pregnancy or those who may become pregnant due to the risk of congenital malformations from excessive vitamin A intake. Patients with hypercalcemia, sarcoidosis (an unknown cause systemic inflammatory disease), or kidney disease should not take this drug. Individuals with allergic reactions to any component in this drug, infants under three months, kidney stone patients, and those allergic to soybean oil, beans, or peanuts should also avoid taking it. Those receiving medical treatment, patients with oxalosis, pregnant or breastfeeding women, premature infants, patients with a history of gout or kidney stones, lipid metabolism disorders, and individuals sensitive to Tartrazine Yellow No. 4 and Yellow No. 5 should consult a specialist before taking this. If symptoms such as nausea, vomiting, itching, dry skin, painful joint swelling, or diarrhea occur during use, discontinue immediately and consult a specialist. Long-term high-dose use may lead to tolerance and pose risks of peptic ulcers, glucose intolerance, hyperuricemia, and liver damage, so caution is needed. Women post-menopause should be cautious with long-term high doses of vitamin A, as it may increase the risk of osteoporosis. Dosage should strictly adhere to prescribed instructions, and since vitamin A is adequately obtained from food, the supplemental dosage should not exceed 5,000 IU per day. This drug may affect blood glucose measurements during urine tests and can change urine color to yellow, affecting clinical test results. Patients with lipid metabolism issues or at risk of lipid overload should regularly monitor plasma lipid levels and adjust dosages if necessary. Keep out of reach of children and store in a sealed container in a cool, dry place away from direct sunlight. To maintain quality, do not transfer to another container and take precautions against misuse.

Side effects and when to seek care immediately

Mild side effects

  • Nausea
  • vomiting
  • itching
  • dry and rough skin
  • painful joint swelling
  • diarrhea
  • loose stools
  • development of tolerance
  • exacerbation of peptic ulcers
  • glucose intolerance
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  • hyperuricemia
  • liver damage
  • increased risk of osteoporosis
  • interference with urine tests
  • yellow discoloration of urine
  • changes in plasma lipid levels.

Not everyone experiences these, and they can vary from person to person.

Interactions

Drug interactions

This drug should be used with intravenous lipid preparations only after consultation with a physician or pharmacist.

Storage

This drug should be stored in a sealed container that can block light, preferably at room temperature between 1 degree and 30 degrees Celsius. Proper storage will maintain the drug's effectiveness and ensure its safe use.

Appearance and packaging

Appearance

Dark green oblong soft capsule containing yellowish-brown contents

Package unit

1 capsule/pack, 600 capsules/box [(1 capsule/pack x 600)]

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

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.

Questions about this medicine

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For anything that needs medical judgment, consult a doctor or pharmacist.

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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.