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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 5 [hp_C]/5 [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
- November 9, 2023
- Manufacturer Document
- Prescribing information, PDF file
- Active ingredient
- Sodium Borate 5 [hp_C]/5 [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
- November 9, 2023
- Manufacturer
- Boiron
- NDC root
- 0220-0888
- 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 can be triggered by factors such as stress, certain foods, or hormonal changes.
These sores typically heal on their own within a week or two, but there are treatments available to help relieve pain and promote healing. If you experience frequent or particularly severe canker sores, it may be helpful to consult with a healthcare professional for further advice and management options.
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, but this treatment aims 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 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 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 advice.
While there are no specific warnings or precautions listed, always stay informed about your health and consult with your healthcare provider if you have any concerns or questions regarding your treatment.
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
It’s important to store this product safely and handle it with care. Always keep it out of reach of children to prevent any accidental ingestion or misuse. 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.
By following these simple guidelines, you can ensure that the product remains safe for use and maintains its quality.
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. Always 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.
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 for children?
Yes, it can be used by both adults and children as directed.
What precautions should I take when using this medication?
Keep it out of reach of children and do not use if the pellet dispenser seal is broken.
What should I do if I am pregnant or breastfeeding?
If you are pregnant or breastfeeding, ask a health professional before use.
Packaging Info
This section summarizes the homeopathic presentations of Borax (sodium borate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Pellet | 5 [hp_C]/5 [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 5 hp_C in 5 hp_C. The formulation includes inactive ingredients such as 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 an item code of NDC: 0220-0888-41, 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 is categorized as an unapproved homeopathic product. The labeler and registrant for this product is Boiron, with the respective identifiers 282560473 and 014892269.
Packaging & NDC
This section summarizes the homeopathic presentations of Borax (sodium borate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Pellet | 5 [hp_C]/5 [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.