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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 1 [hp_M]/1 [hp_M]
- 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
- November 9, 2023
- Manufacturer Document
- Prescribing information, PDF file
- Active ingredient
- Sodium Borate 1 [hp_M]/1 [hp_M]
- 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
- November 9, 2023
- Manufacturer
- Boiron
- NDC root
- 0220-0877
- 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 isn't fully understood, they are commonly triggered by factors such as stress, certain foods, or minor injuries to the mouth.
These sores typically heal on their own within one to two weeks. While there are treatments available to help relieve pain and promote healing, it's important to consult with a healthcare professional if you experience frequent or severe canker sores.
Uses
You may use this medication to help treat canker sores, which are painful, small 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 this medication does not have any known effects that could harm a developing fetus (teratogenic effects), so it is considered safe in that regard. If you have any questions or concerns about using this medication, be sure to consult with your healthcare provider.
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 from under your tongue. Remember to follow your doctor's instructions if they provide specific guidance on how long to continue this treatment.
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 prioritize your health and safety. If you have any concerns or experience unusual side effects, don't hesitate to reach out to your healthcare provider for advice.
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 extreme 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
It’s important to store this product safely to ensure its effectiveness. Always keep it out of reach of children to prevent accidental use. Before using, check that the seal on the pellet dispenser is intact; do not use the product if the seal is broken, as this could compromise its safety and effectiveness.
When handling the product, make sure to follow any additional safety guidelines provided. Proper storage and careful handling will help you use the product safely and effectively.
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 last 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 are canker sores?
Canker sores are small, painful ulcers that can occur in the mouth.
How should I take 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.
What should I do if my symptoms persist?
Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.
Is this medication safe to use during pregnancy or breastfeeding?
If you are pregnant or breastfeeding, ask a health professional before use.
What precautions should I take when using this medication?
Keep this medication out of reach of children and do not use 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 | 1 [hp_M]/1 [hp_M] | ||
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 1 hp_M in 1 hp_M. Inactive ingredients include lactose (UNII: J2B2A4N98G) and sucrose (UNII: C151H8M554). The product is characterized by a white color, round shape, and a size of 4 mm. It is packaged in a tube, with the item code NDC: 0220-0877-41, and is classified as a Type 0 product, indicating it is not a combination product. The marketing start date for this product is March 3, 1983, and it falls under the category of unapproved homeopathic products.
Packaging & NDC
This section summarizes the homeopathic presentations of Borax (sodium borate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Pellet | 1 [hp_M]/1 [hp_M] | ||
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.