Medication info
Power Vita Soft Capsule

Power Vita 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 capsuleVitamin A Oil›5mg / 1 capsule
Manufacturer / importer
(주)바스칸바이오제약
Appearance
An elongated soft capsule with dark green color containing brownish-yellow contents
Packaging
1 capsule/pack, 500 capsules/box [(1 capsule/pack x 500)]
Approval status
Active

MFDS item code 201607393 · Notified 2016.12.30

Summary

Main use
Improves physical fatigue, alleviates dry eyes during pregnancy and lactation, and enhances bone development
Who takes it
Adults
Adult dose
1 capsule once a day for adults

Ingredients

Manufacturer
(주)바스칸바이오제약

Efficacy & effects

Improves physical fatigue, alleviates dry eyes during pregnancy and lactation, and enhances bone development

  • Physical fatigue
  • reduced stamina
  • dry eyes
  • night blindness
  • poor bone development
  • poor dental development
View approved original text

The vitamins A, D, B1, B2, and C included in this medication support physical functions during periods of physical fatigue, pregnancy, lactation, and when energy is depleted during or following illness, as well as during growth and old age. Additionally, vitamin A helps to reduce dry eyes and assists in the treatment of night blindness. Vitamin D aids in the healthy development of bones and teeth, and is effective in preventing rickets. This medicine is used to improve nutritional balance throughout the body and enhance vision and bone health.

How to take

Adult dose

1 capsule once a day for adults

Precautions

This medication should be used with caution in women during the first three months of pregnancy or those who may become pregnant due to the risk of congenital anomalies from excessive vitamin A intake. Unless a patient suffers from vitamin A deficiency, daily intake of more than 5,000 IU should be avoided. Patients with hypercalcemia, sarcoidosis (a systemic inflammatory disease of unknown origin), or kidney disease should not take this medication. If allergic or hypersensitive to any of the components in this medication, infants younger than 3 months, patients with kidney stones, or those allergic to soybean oil, peanuts, or soy should also avoid taking this medication. Patients under medical treatment or with lipid metabolism disorders, such as oxalate nephropathy, gout, hyperlipoproteinemia, diabetic dyslipidemia, or pancreatitis, should consult a specialist before use. Pregnant or nursing women, premature infants, and babies must consult healthcare professionals before use. This medication contains Yellow No. 4 and Yellow No. 5 dyes; caution is advised for those allergic to these components. If symptoms such as nausea, vomiting, skin itching, dryness, joint swelling, or diarrhea occur during use, discontinue immediately and consult a specialist. Long-term high-dose use may lead to tolerance, and conditions such as peptic ulcers, liver damage, blood glucose control issues, and hyperuricemia may occur, so caution is required. If symptoms do not improve after overdose or use for more than one month, discontinue use and consult a specialist. The defined usage and dosage must be strictly followed, as vitamin A can also be adequately obtained through diet. Therefore, vitamin A intake should not exceed 5,000 IU as a supplement. This medication may affect blood glucose levels during urine tests and can change urine color to yellow, impacting clinical test results. Patients at risk of fat overload should regularly monitor plasma lipid levels and adjust the dosage of this medication as necessary. Store out of reach of children, avoiding direct sunlight, and keep it tightly sealed in a cool, dry place. For quality maintenance, do not transfer to other containers.

Side effects and when to seek care immediately

Mild side effects

Nausea, vomiting, itching, dry and rough skin, painful joint swelling, diarrhea, loose stools, potential for tolerance, exacerbation of peptic ulcers, impairment of glucose tolerance, hyperuricemia, liver damage, increased risk of osteoporosis, interference with blood glucose detection, yellow discoloration of urine, risk associated with fat overload.

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

Interactions

Drug interactions

Consult with a physician or pharmacist before using this medication with injectable lipid preparations.

Storage

This medication should be stored in a closed container that is not exposed to light, ideally at room temperature between 1℃ and 30℃. Storing it this way helps maintain its efficacy and prevent deterioration.

Appearance and packaging

Appearance

An elongated soft capsule with dark green color containing brownish-yellow contents

Package unit

1 capsule/pack, 500 capsules/box [(1 capsule/pack x 500)]

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.