ADD CONDITION
Borax
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_X]
- 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
- August 29, 2023
- Manufacturer Document
- Prescribing information, PDF file
- Active ingredient
- Sodium Borate 6 [hp_X]
- 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
- August 29, 2023
- Manufacturer
- Boiron
- NDC root
- 0220-0887
- 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. While the exact cause of canker sores is not fully understood, they are commonly triggered by factors such as stress, certain foods, or minor injuries to the mouth.
If you experience canker sores, it's important to know that they are generally not contagious and usually heal on their own within a week or two. There are various treatments available to help relieve pain and promote healing, so you may want to consult with a healthcare professional for advice tailored to your situation.
Uses
You can use this medication to help treat canker sores, which are painful, small ulcers that can appear inside your mouth. These sores can make eating and speaking uncomfortable, but this treatment is designed to alleviate that discomfort and promote healing.
It's important to note that this medication has not been shown to cause any birth defects (teratogenic effects) or other harmful effects during pregnancy. Always consult with your healthcare provider for personalized advice and to ensure this treatment is right for you.
Dosage and Administration
When you start experiencing symptoms, take 5 pellets of the medication and let them dissolve under your tongue. You should do this three times a day. Continue taking the pellets until your symptoms improve or follow your doctor's instructions if they provide different guidance.
This method of administration is simple and effective, allowing the medication to be absorbed quickly into your system. Remember, it's important to stick to the recommended dosage and frequency for the best results.
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 laboratory tests mentioned, always stay vigilant about how you feel while on any medication. If you experience any unusual or concerning symptoms, don't hesitate to reach out to your healthcare provider. Your health and safety are paramount.
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. Remember, timely intervention can make a significant difference.
Storage and Handling
To ensure the safety and effectiveness of your product, always keep it out of reach of children. This helps prevent accidental ingestion or misuse. Additionally, do not use the product if the seal on the pellet dispenser is broken, as this could indicate that the product is compromised and may not work as intended.
By following these simple guidelines, you can help ensure that the product remains safe for use and functions properly.
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 ask a healthcare professional before using this product. Keep it out of reach of children and do not use it if the seal on the pellet dispenser is broken.
FAQ
What are canker sores?
Canker sores are small, painful ulcers that can occur in the mouth.
How should I use this medication for canker sores?
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 medication?
No teratogenic effects have been mentioned for this medication.
What should I do if my symptoms persist?
Stop use and ask a doctor if your symptoms persist for more than 3 days or worsen.
Is this medication safe for children?
Yes, but keep it out of reach of children and follow the dosage instructions.
What precautions should I take when using this medication?
Do not use if the pellet dispenser seal is broken, and consult a health professional if you are pregnant or breastfeeding.
Packaging Info
This section summarizes the homeopathic presentations of Borax (sodium borate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Pellet | 6 [hp_X] | ||
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 Borax (Sodium Borate) as the active ingredient at a strength of 6X, 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 packaged in a tube containing approximately 80 pellets and is intended for oral administration. The item code (NDC) is 0220-0887, and it is labeled by Boiron, with marketing commencing on March 3, 1983.
Packaging & NDC
This section summarizes the homeopathic presentations of Borax (sodium borate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Pellet | 6 [hp_X] | ||
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.