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Ustilago Maidis

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DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Active ingredient
Ustilago Maydis 200 [kp_C]/200 [kp_C]
Drug class
Non-Standardized Fungal Allergenic Extract
Dosage form
Pellet
Route
Oral
Prescription status
Homeopathic
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2024
Label revision date
July 29, 2024
Manufacturer
Boiron
NDC root
0220-5154

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Drug Overview

If you experience heavy menstruation, there is a medication designed to help relieve this condition. This drug works by addressing the symptoms associated with heavy menstrual bleeding, providing support during your menstrual cycle. It is important to consult with a healthcare professional to determine if this medication is right for you and to understand how it can best meet your needs.

Uses

If you experience heavy menstruation, this medication can help relieve your symptoms. It is specifically designed to address this issue, providing you with comfort during your menstrual cycle.

Rest assured, there are no known teratogenic effects (which means it does not cause birth defects) associated with this medication, making it a safer option for those concerned about such risks.

Dosage and Administration

When you first notice symptoms, take 5 pellets of the medication and let them dissolve under your tongue. You should do this three times a day. Continue this routine until your symptoms improve or follow your doctor's specific instructions. This method helps ensure that the medication is absorbed quickly into your system for effective relief.

Warnings and Precautions

It's important to be aware of how to use this medication safely. If your symptoms last more than three days or get worse, you should stop taking the medication and contact your doctor for further advice.

While there are no specific warnings or precautions listed, always stay vigilant about how you feel while using any medication. If you experience any unusual symptoms or have concerns, don't hesitate to reach out to your healthcare provider. Your health and safety are the top priority.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While there is no specific information available about the signs of overdose for this medication, general symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, seek medical help right away.

In case of an overdose, contact your local emergency services or go to the nearest hospital. It's always better to err on the side of caution when it comes to your health. Remember, timely intervention can make a significant difference.

Storage and Handling

To ensure the best performance of your product, store it at room temperature. It's important to check the pellet dispenser before use; do not use it if the seal is broken, as this could compromise the safety and effectiveness of the device. Always handle the product with care to maintain its integrity and ensure safe usage.

Additional Information

No further information is available.

FAQ

What is the primary use of this drug?

This drug is used to relieve heavy menstruation.

How should I take this medication?

At the onset of symptoms, dissolve 5 pellets under your tongue 3 times a day until symptoms are relieved or as directed by a doctor.

Are there any teratogenic effects associated with this drug?

No teratogenic effects (causing malformations in a developing fetus) are mentioned.

What should I do if my symptoms persist?

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.

How should I store this medication?

Store the medication at room temperature and do not use it if the pellet dispenser seal is broken.

Packaging Info

This section summarizes the homeopathic presentations of Ustilago Maidis (ustilago maydis). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Ustilago Maidis.
Details

Manufacturer Insert (PDF)

This file includes usage instructions and other product details provided by the manufacturer. This is not an FDA-approved drug.

View manufacturer document (PDF)

Description

Description:

This product contains Ustilago maidis 200CK as the active ingredient, with a strength of 0.443 mg per pellet. The active ingredient is also recognized in the Homeopathic Pharmacopoeia of the United States (HPUS) as Ustilago maidis 200CK HPUS. Inactive ingredients include lactose (unspecified form) and sucrose. The pellets are characterized by a turquoise color, round shape, and a size of 4 mm. The product is packaged under Item Code NDC: 0220-5154-41, with a package description of 200 pellets in 1 tube; it is classified as Type 0: Not a Combination Product. The route of administration is oral.

Packaging & NDC

This section summarizes the homeopathic presentations of Ustilago Maidis (ustilago maydis). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Ustilago Maidis.
Details

Manufacturer Insert (PDF)

This is the product document submitted by Boiron for Ustilago Maidis. It includes information on ingredients, suggested use, and labeling language. This product is not FDA-approved.

View product insert (PDF)

Data Generation & Sources

This page was automatically generated and is maintained by the AllDrugs AI Data-Science Team. It was built from the manufacturer-supplied FDA Structured Product Label (DailyMed) for Ustilago Maidis, retrieved by a validated AI data-extraction workflow.

All dosage forms and strengths provided by the manufacturer are listed in the Packaging & NDC Codes section above.

Homeopathic drug products are not reviewed by FDA for safety or effectiveness; information is reproduced without modification.

No human clinician has reviewed this version.

Learn more in our Editorial Policy

Last AI update:

Primary FDA sources:

Orange Book data shown on this page are limited to Regulatory Status (Rx), Established Pharmacologic Class (EPC), and Mechanism of Action (MoA).

Regulatory data notice: Information on this page is reproduced verbatim from FDA public databases (NSDE, Orange Book, Purple Book, DailyMed SPL). NDA/ANDA drugs are FDA-approved, BLA biologics are FDA-licensed. Inclusion alone does not guarantee current market availability or imply FDA endorsement.

Medical disclaimer: This AI-generated content is provided for educational purposes only and does not constitute medical advice. Always consult a licensed healthcare professional for diagnosis or treatment decisions.