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Borax
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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
- Sodium Borate 15 [hp_C]/15 [hp_C]
- Other brand names
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Hahnemann Laboratories, Inc.)
- Borax (by Ohm Pharma Inc.)
- Borax (by Rxhomeo Private Limited D. B. a. Rxhomeo, Inc)
- Borax (by Rxhomeo Private Limited D. B. a. Rxhomeo, Inc)
- Borax (by Rxhomeo Private Limited D. B. a. Rxhomeo, Inc)
- Borax (by Sevene Usa)
- Borax (by Sevene Usa)
- Borax (by Warsan Homeopathic)
- Borax (by Warsan Homeopathic)
- Borax 30c (by Paramesh Banerji Life Sciences Llc)
- View full label-group details →
- Dosage form
- Pellet
- Route
- Oral
- Prescription status
- Homeopathic
- Marketed in the U.S.
- Since 1983
- Label revision date
- October 17, 2023
- Manufacturer Document
- Prescribing information, PDF file
- Active ingredient
- Sodium Borate 15 [hp_C]/15 [hp_C]
- Other brand names
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Boiron)
- Borax (by Hahnemann Laboratories, Inc.)
- Borax (by Ohm Pharma Inc.)
- Borax (by Rxhomeo Private Limited D. B. a. Rxhomeo, Inc)
- Borax (by Rxhomeo Private Limited D. B. a. Rxhomeo, Inc)
- Borax (by Rxhomeo Private Limited D. B. a. Rxhomeo, Inc)
- Borax (by Sevene Usa)
- Borax (by Sevene Usa)
- Borax (by Warsan Homeopathic)
- Borax (by Warsan Homeopathic)
- Borax 30c (by Paramesh Banerji Life Sciences Llc)
- View full label-group details →
- Dosage form
- Pellet
- Route
- Oral
- Prescription status
- Homeopathic
- CSA schedule
- Not a scheduled drug
- Marketed in the U.S.
- Since 1983
- Label revision date
- October 17, 2023
- Manufacturer
- Boiron
- NDC root
- 0220-0880
- Manufacturer Document
- Prescribing information, PDF file
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
Canker sores are small, painful ulcers that can develop inside your mouth, often making eating and speaking uncomfortable. They are a common condition and can be triggered by various factors, including stress, certain foods, or hormonal changes. While the exact cause of canker sores is not fully understood, they typically heal on their own within a week or two.
If you experience canker sores, there are treatments available that can help alleviate pain and promote healing. It's important to consult with a healthcare professional for advice tailored to your specific situation.
Uses
You may use this medication to help treat canker sores, which are painful ulcers that can develop inside your mouth. These sores can make eating, drinking, and talking uncomfortable. If you're experiencing canker sores, this treatment can provide relief and help speed up the healing process.
It's important to note that there are no known teratogenic effects (harmful effects on a developing fetus) associated with this medication, making it a safer option for those who are pregnant or planning to become pregnant.
Dosage and Administration
When you first notice symptoms, take 5 pellets 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 is suitable for both adults and children, ensuring that everyone can find relief when they need it.
Warnings and Precautions
It's important to be aware of certain precautions when using this medication. 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 emergency instructions provided, always prioritize your health and seek medical attention if you have any concerns about your condition or the medication you are taking. Regular communication with your healthcare provider is key to ensuring your safety and well-being.
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, 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 always better to be safe and get checked by a healthcare professional if you have any concerns about your health.
Storage and Handling
To ensure the safety and effectiveness of your product, always keep it out of reach of children. It's important to check the pellet dispenser before use; do not use the product if the seal is broken, as this could indicate that the product is compromised. Following these guidelines will help you handle the device safely and maintain its integrity.
Additional Information
You should take this medication orally. For both adults and children, dissolve 5 pellets under your tongue three times a day at the onset of symptoms, continuing until symptoms improve or as directed by your doctor.
If your symptoms persist for more than three days or worsen, stop using the medication and consult your doctor. If you are pregnant or breastfeeding, it's important to speak with a healthcare professional before using this product. Always keep it out of reach of children and do not use it if the pellet dispenser seal is broken.
FAQ
What is the drug used for?
This drug is used for the treatment of canker sores.
How should I use 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 your doctor.
Are there any warnings associated with this drug?
You should stop use and ask a doctor if symptoms persist for more than 3 days or worsen.
What should I do if I am pregnant or breastfeeding?
If you are pregnant or breastfeeding, ask a health professional before use.
How should I store this medication?
Keep this medication out of reach of children and do not use it if the pellet dispenser seal is broken.
Packaging Info
This section summarizes the homeopathic presentations of Borax (sodium borate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Pellet | 15 [hp_C]/15 [hp_C] | ||
Product details Regulatory status — Marketed All current FDA data sets list this NDC as actively marketed. FDA record dates for this NDC:
Active ingredients
Inactive ingredients
| ||||
Manufacturer Insert (PDF)
This file includes usage instructions and other product details provided by the manufacturer. This is not an FDA-approved drug.
Description
Description:
This product contains Sodium borate as the active ingredient, with a strength of 15C, providing 0.443 mg of the active ingredient per pellet. The inactive ingredients include lactose and sucrose. The product is characterized by its white color, round shape, and a size of 4 mm. It is administered orally and classified as a human over-the-counter (OTC) drug. The National Drug Code (NDC) for this product is 0220-0880, and it is packaged with 15 pellets in one tube. This product is not a combination product. The marketing start date is March 3, 1983, and it is labeled by Boiron (NDC: 0220-0880-41), with Boiron, Inc. serving as the registrant (014892269).
Packaging & NDC
This section summarizes the homeopathic presentations of Borax (sodium borate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Pellet | 15 [hp_C]/15 [hp_C] | ||
Product details Regulatory status — Marketed All current FDA data sets list this NDC as actively marketed. FDA record dates for this NDC:
Active ingredients
Inactive ingredients
| ||||
Manufacturer Insert (PDF)
This is the product document submitted by Boiron for Borax. It includes information on ingredients, suggested use, and labeling language. This product is not FDA-approved.