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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 6 [hp_C]/6 [hp_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 1983
Label revision date
July 29, 2024
Manufacturer
Boiron
NDC root
0220-5156

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Drug Overview

If you experience heavy menstruation, there is a medication designed to help relieve this condition. This drug works specifically to address the symptoms associated with heavy menstrual bleeding, providing support during your menstrual cycle. While the exact mechanism of action isn't detailed, its primary purpose is to help manage and alleviate the discomfort that can come with heavy periods.

Uses

If you experience heavy menstruation, this medication can help relieve your symptoms. It's designed to make your menstrual flow more manageable, allowing you to feel more comfortable during your period.

Rest assured, this medication does not have any teratogenic effects, meaning it does not cause birth defects if taken during pregnancy.

Dosage and Administration

When you start experiencing symptoms, take 5 pellets of the medication and place them under your tongue. Allow the pellets to dissolve completely. You should do this three times a day until your symptoms improve or as your doctor advises.

This method of taking the medication is called sublingual administration, which means it is absorbed directly into your bloodstream through the tissue under your tongue. Following this routine will help ensure you get the most benefit from the treatment.

Warnings and Precautions

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

While there are no specific warnings or precautions mentioned, always stay vigilant about how you feel while using any medication. If you have any concerns or experience unusual symptoms, 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 the specific signs of an overdose are not detailed, common symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, or if you are unsure, seek medical help right away.

In case of an overdose, contact your local emergency services or go to the nearest hospital. It's crucial to provide them with as much information as possible about the substance taken and the amount, if known. Remember, acting quickly can make a significant difference in your health and safety.

Storage and Handling

To ensure the best performance of your product, store it at room temperature. It's important to keep it in a stable environment, away from extreme heat or cold. Additionally, always check the pellet dispenser before use; do not use the product if the seal is broken, as this could compromise its safety and effectiveness.

By following these simple storage and handling guidelines, you can help maintain the quality and reliability of your device.

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?

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

What should I do if my symptoms persist?

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

Are there any teratogenic effects associated with this drug?

No teratogenic effects are mentioned for this drug.

What precautions should I take when using 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 6C as the active ingredient, with a strength of 0.443 mg per pellet. The active ingredient is recognized in the Homeopathic Pharmacopoeia of the United States (HPUS) as Ustilago maidis 6C HPUS. The pellets are formulated for oral administration and are classified as a human over-the-counter (OTC) drug. Each pellet is round, white in color, and measures 4 mm in size. Inactive ingredients include lactose and sucrose. The ingredient name is Ustilago maydis (UNII: 4K7Z7K7SWG), with a strength designation of Ustilago maydis 6 hp_C in 6 hp_C.

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.