Product image of Natrovit (Retinol Palmitate, Ascorbic Acid, Colecalciferol, Cyanocobalamin, Dexpanthenol, Folic Acid, Nicotina) supplied by GNH India

Natrovit

Active Ingredient:
Retinol Palmitate, Ascorbic Acid, Colecalciferol, Cyanocobalamin, Dexpanthenol, Folic Acid, Nicotina
Origin:
EU

Natrovit (Retinol Palmitate, Ascorbic Acid, Colecalciferol, Cyanocobalamin, Dexpanthenol, Folic Acid, Nicotina)

Retinol Palmitate, Ascorbic Acid, Colecalciferol, Cyanocobalamin, Dexpanthenol, Folic Acid, Nicotina, the active ingredients in Natrovit, are a multivitamin supplement presented as a sterile intravenous solution for parenteral use. It supports prevention of vitamin deficiencies and provides nutritional support in clinical settings.

GNH India supplies Natrovit as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Noridem Enterprises Ltd

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Indications & Clinical Uses

Natrovit, a multivitamin supplement, addresses vitamin deficiency and supports metabolic pathways that require essential micronutrients.

  • Vitamin deficiency prevention: helps restore adequate levels of essential vitamins in patients at risk of deficiency.
  • Parenteral nutrition support: provides necessary micronutrients when oral intake is insufficient or contraindicated.
  • Post‑operative recovery: assists in meeting increased metabolic demands after surgery.

How It Works

  • The components of Natrovit act as co‑enzymes, antioxidants and hormone precursors that participate in cellular metabolism. Retinol palmitate supports visual and epithelial health, ascorbic acid scavenges free radicals, colecalciferol regulates calcium homeostasis, cyanocobalamin and folic acid are essential for DNA synthesis, dexpanthenol aids tissue repair, and nicotine influences neurotransmission. Together they replenish depleted stores and facilitate normal biochemical pathways.

Side Effects

Natrovit may be associated with a range of adverse reactions following intravenous administration.

Common Side Effects

  • Infusion site erythema: mild redness at the injection site.
  • Nausea: transient feeling of queasiness.
  • Headache: mild to moderate headache.
  • Flushing: temporary warmth and reddening of skin.
  • Mild hypervitaminosis symptoms: such as transient fatigue.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypervitaminosis D: risk of hypercalcemia with excessive dosing.
  • Liver enzyme elevation: possible hepatic stress.
  • Severe hypersensitivity rash: extensive skin eruption.
  • Thromboembolic events: rare clot formation.

Precautions & Warnings

When using Natrovit, clinicians should consider several safety measures.

  • Assess baseline vitamin levels: evaluate patient status before infusion.
  • Monitor for hypersensitivity: watch for rash, itching or respiratory distress.
  • Avoid in known hypersensitivity: do not administer to patients allergic to any component.
  • Use caution in renal or hepatic impairment: adjust monitoring as needed.
  • Pregnancy and lactation: limited data; use only if clearly indicated.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Natrovit can interact with other medicines; awareness of major and moderate interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • High‑dose vitamin A with isotretinoin: increased risk of toxicity.
  • Vitamin D with thiazide diuretics: potential hypercalcemia.
  • Cyanocobalamin with metformin: reduced B12 absorption.
  • Folic acid with methotrexate: may diminish methotrexate efficacy.

Moderate Interactions (Monitor Closely)

  • Ascorbic acid with iron supplements: enhanced iron absorption.
  • Dexpanthenol with cholinergic agents: possible potentiation of effects.
  • Nicotine with nicotine replacement therapy: additive sympathomimetic activity.

Frequently Asked Questions

Natrovit is an intravenous multivitamin formulation used to prevent vitamin deficiencies and to provide nutritional support in clinical settings such as parenteral nutrition, postoperative care, and patients unable to meet their micronutrient needs orally.

Each ingredient serves a specific biological role: retinol palmitate supports vision and skin health; ascorbic acid acts as an antioxidant; colecalciferol regulates calcium metabolism; cyanocobalamin and folic acid are essential for DNA synthesis; dexpanthenol aids tissue repair; and nicotine influences neurotransmission. Together they replenish essential cofactors required for normal metabolic functions.

The dosing regimen for Natrovit is determined by the prescribing clinician based on the patient’s clinical condition, laboratory results and nutritional requirements. Healthcare professionals should follow institutional protocols and adjust the dose as needed.

Safety data for Natrovit in pregnancy and lactation are limited. It should only be used when clearly indicated and after a risk‑benefit assessment by the treating physician. Consultation with obstetric specialists is recommended.

To order Natrovit, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if required) and necessary import documentation.

Natrovit combines a broad spectrum of vitamins and a nicotine component in a single sterile solution, offering comprehensive micronutrient coverage. Compared with single‑vitamin IV products, it reduces the need for multiple infusions, but clinicians should consider individual patient needs and potential interactions when selecting a formulation.

Natrovit must be stored at 2‑8 °C, protected from light, and kept in its original container. Do not freeze or shake the product. Before administration, allow the solution to reach room temperature if required by institutional policy.

Natrovit is given by intravenous infusion under aseptic conditions. The rate and volume of infusion are set by the healthcare professional according to the patient’s age, weight, clinical status and institutional guidelines.

Serious risks include anaphylactic reactions, severe hypervitaminosis (particularly vitamin D‑related hypercalcemia), liver enzyme elevation and rare thromboembolic events. Immediate medical attention is required if any signs of severe allergy or organ dysfunction appear.

Natrovit should be avoided in patients with known hypersensitivity to any of its components, in those with uncontrolled hypercalcemia, severe liver disease, or in individuals where the risk of vitamin toxicity outweighs the benefit. Clinical judgment is essential.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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