Symptom checker
Select audience type

Switch between content for healthcare professionals (PRO) and general audience (GEN).

ADD CONDITION

items per page

Sodium borate

Last content change checked dailysee data sync status

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
Sodium Borate 6 [hp_C]/6 [hp_C]
Other brand names
Dosage form
Pellet
Route
Oral
Prescription status
Homeopathic
Marketed in the U.S.
Since 2019
Label revision date
December 29, 2021
Manufacturer Document
Prescribing information, PDF file
Active ingredient
Sodium Borate 6 [hp_C]/6 [hp_C]
Other brand names
Dosage form
Pellet
Route
Oral
Prescription status
Homeopathic
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2019
Label revision date
December 29, 2021
Manufacturer
OHM PHARMA INC.
NDC root
66096-800
Manufacturer Document
Prescribing information, PDF file
Packaging Info
Packaging & NDC Codes

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

If you are a consumer or patient please visit this version.

Drug Overview

Borax is a homeopathic remedy available in various potencies, including Borax 6X-30X, 3C-30C, 200C, and 1M. It is used according to standard homeopathic indications, which means it is intended to support the body's natural healing processes. Typically, Borax is offered in dilution forms, with standard bottle sizes ranging from 30mL to 60mL.

Uses

You can use this medication according to standard homeopathic indications, which means it is intended to help with various health concerns based on homeopathic principles.

It's important to note that there are no reported teratogenic effects (which means it does not cause birth defects) or nonteratogenic effects associated with this medication. This suggests that it is considered safe in these aspects. Always consult with a healthcare professional for personalized advice and to ensure this treatment is right for you.

Dosage and Administration

To take your medication, you will need to dissolve 3 to 5 pellets under your tongue. This method is known as sublingual administration, which means the medication is absorbed directly into your bloodstream through the tissues under your tongue. You should do this three times a day, or follow the specific instructions given by your healthcare professional.

Make sure to let the pellets fully dissolve for the best effect. If you have any questions about how to take your medication or if you need to adjust the dosage, don’t hesitate to reach out to your doctor or pharmacist for guidance.

Warnings and Precautions

It's important to keep this medication out of reach of children to prevent accidental ingestion. If you are pregnant or breastfeeding, please consult a healthcare professional before using this product to ensure it is safe for you and your baby.

If your symptoms last longer than three days or worsen, stop using the medication and reach out to a healthcare professional for guidance. Always prioritize your health and safety by seeking help when needed.

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 effects of an overdose for this medication, you should be aware of general signs that may indicate a problem. These can include unusual drowsiness, confusion, or difficulty breathing.

If you notice any of these symptoms or if you believe you have taken too much of the medication, seek medical help right away. Contact your healthcare provider or go to the nearest emergency room. It's always better to be safe and get checked out if you have any concerns about your health.

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 Borax?

Borax is an over-the-counter (OTC) homeopathic remedy available in various potencies, including 6X-30X, 3C-30C, 200C, and 1M.

How should I use Borax?

You should use Borax according to standard homeopathic indications, typically dissolving 3-5 pellets under your tongue three times a day or as directed by a professional.

Are there any teratogenic effects associated with Borax?

No teratogenic effects have been mentioned for Borax.

Are there any nonteratogenic effects associated with Borax?

No nonteratogenic effects have been mentioned for Borax.

What precautions should I take when using Borax?

Keep Borax out of reach of children, and if you are pregnant or breastfeeding, consult a healthcare professional before use.

What should I do if symptoms persist or worsen?

You should stop using Borax and consult a healthcare professional if symptoms persist for more than three days or worsen.

How should I store Borax?

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

Packaging Info

This section summarizes the homeopathic presentations of Borax. Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Borax.
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 Borax as the active ingredient, specifically Sodium Borate (UNII: 91MBZ8H3QO), with a strength of 6 hp_C in 6 hp_C. Each package contains approximately 100 pellets, which are round, white, and measure 4 mm in size. The inactive ingredients include organic sucrose and are lactose-free. The product is manufactured in accordance with the Homeopathic Pharmacopoeia of the United States (HPUS) and is intended for oral administration. It is packaged in a tube, with the item code NDC: 66096-800-01, and is classified as an unapproved homeopathic product. The marketing start date for this product is November 1, 2019.

Packaging & NDC

This section summarizes the homeopathic presentations of Borax. Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Borax.
Details

Manufacturer Insert (PDF)

This is the product document submitted by OHM PHARMA INC. for Borax. 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 Borax, 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.