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Dinost Dinoprostone Gel 0.5mg
Dinost Dinoprostone Gel 0.5mg

Dinost Dinoprostone Gel 0.5mg

Dinost Dinoprostone Gel 0.5mg Specification

  • CAS No
  • 363-24-6
  • Grade
  • Pharmaceutical Grade
  • Molecular Formula
  • C20H32O5
  • Application
  • Hospital, Clinical
  • Purity
  • 99%
  • Formulations Type
  • General Drugs
  • Formulations Form
  • Gel
  • Treatments & Functions
  • Induction of labor, cervical ripening
  • Gender/Age Group
  • Adult
  • Dosage Guidelines
  • As directed by physician
  • Volume
  • 3 g
  • Storage Instructions
  • Store in a cool, dry place below 25C
  • Safety Information
  • Use under medical supervision only
  • Active Ingredient
  • Dinoprostone
  • Prescription
  • Prescription required
  • Colour
  • Transparent
  • Brand Name
  • Dinost
  • Strength
  • 0.5 mg
  • Packaging Type
  • Pre-filled syringe
  • Usage
  • For vaginal administration only
  • Expiry
  • 24 Months
  • Contraindications
  • Not for use in hypersensitivity to prostaglandins
 

Dinost Dinoprostone Gel 0.5mg Trade Information

  • Supply Ability
  • 1000 Per Day
  • Delivery Time
  • 7 Days
  • Sample Available
  • No
  • Sample Policy
  • Contact us for information regarding our sample policy
 

About Dinost Dinoprostone Gel 0.5mg

Strength
0.5 mg
Packaging Size
3.0g
Packaging Type
Box
Composition
Dinoprostone Gel
Usage/Application
Hospital
Shelf Life
24 Months
Brand
Dinost
Treatment
Used To Help Prepare Your Cervix
Dinost 0.5mg Gelcontains a natural substance (prostaglandin) called Dinoprostone, that your body makes in preparation for labour or delivery of a full term baby. It softens and widens the opening of the womb and increases contractions of the uterus.


Effective Labor Induction Solution

Dinost Dinoprostone Gel is engineered for precise and controlled vaginal administration, helping healthcare professionals induce labor or achieve cervical ripening safely. Its pre-filled syringe simplifies the application procedure, ensuring dose accuracy and reducing preparation time during clinical procedures.


Safe and Monitored Application

The gel's use in adults requires supervision by qualified medical staff within hospital or clinical environments. Its pharmaceutical-grade purity and controlled formulation minimize risks of complications. Comprehensive contraindication screening and storage recommendations underscore the medication's commitment to patient safety.

FAQ's of Dinost Dinoprostone Gel 0.5mg:


Q: How should Dinost Dinoprostone Gel 0.5mg be administered?

A: Dinost Dinoprostone Gel is intended solely for vaginal administration by a medical professional. The pre-filled syringe enables easy and accurate delivery of the medication in clinical or hospital settings.

Q: What is the primary benefit of using Dinost Dinoprostone Gel 0.5mg?

A: This gel is primarily used to induce labor and prepare the cervix for childbirth. Its controlled delivery helps healthcare providers achieve effective labor induction and cervical ripening, optimising patient outcomes.

Q: When must Dinost Dinoprostone Gel not be used?

A: Dinost should not be administered to individuals with hypersensitivity to prostaglandins, as this can lead to severe adverse reactions. Always undergo a thorough screening before use.

Q: Where should the Dinost Dinoprostone Gel be stored?

A: This gel must be stored in a cool, dry place below 25C to maintain stability and efficacy. Proper storage conditions are critical to prevent degradation of the active ingredient.

Q: What process ensures the safe use of Dinost Dinoprostone Gel?

A: Safe application of Dinost gel involves medical supervision throughout administration, careful adherence to dosage instructions, and observance of contraindications to avoid any risks associated with improper use.

Q: Who can use Dinost Dinoprostone Gel 0.5mg?

A: Dinost gel is intended for adult women under prescription and medical supervision, typically within hospital or clinical environments for labor induction or cervical ripening.

Q: What are the usage guidelines for Dinost Dinoprostone Gel?

A: Usage and dosage must be determined by a physician. The gel is administered by healthcare professionals exclusively within appropriate clinical or hospital settings to ensure patient safety.

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