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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 30 [hp_X]/30 [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
- November 9, 2023
- Manufacturer Document
- Prescribing information, PDF file
- Active ingredient
- Sodium Borate 30 [hp_X]/30 [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
- November 9, 2023
- Manufacturer
- Boiron
- NDC root
- 0220-0892
- 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.
These sores typically heal on their own within one to two weeks. While there is no specific medication to cure canker sores, various treatments can help relieve pain and promote healing. If you experience frequent or particularly severe canker sores, it may be helpful to consult a healthcare professional for advice and management options.
Uses
If you're dealing with canker sores, this medication can help you find relief. Canker sores are painful, small ulcers that can appear inside your mouth, making it uncomfortable to eat or speak. This treatment is specifically indicated for managing these sores, helping to alleviate the discomfort they cause.
It's important to note that there are no known teratogenic effects (harmful effects on a developing fetus) associated with this medication, so it is considered safe in that regard. If you're experiencing canker sores, this medication may be a suitable option for you.
Dosage and Administration
When you start experiencing 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, making it easy to manage your symptoms effectively.
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 vigilant about how you feel while using any medication. If you experience any unusual symptoms or reactions, it's best to consult with your healthcare provider.
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, 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, 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 and may not work as intended.
By following these simple guidelines, you can help ensure that the product remains safe and effective for your use.
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 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.
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 during pregnancy or breastfeeding?
If you are pregnant or breastfeeding, ask a health professional before use.
What precautions should I take with this medication?
Keep this medication out of reach of children and do not use if the pellet dispenser seal is broken.
Are there any warnings associated with this medication?
No specific warnings are provided, but you should consult a doctor if you have concerns.
Packaging Info
This section summarizes the homeopathic presentations of Borax (sodium borate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Pellet | 30 [hp_X]/30 [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 Sodium borate as the active ingredient at a strength of 30 hp_X. It is formulated as an oral dosage form, presented in a round shape with a white appearance and a size of 4 mm. Each package contains approximately 80 pellets. Inactive ingredients include lactose and sucrose. The product is packaged in a tube, identified by the item code NDC: 0220-0892-41. It is classified as an unapproved homeopathic product, with a marketing start date of 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 | 30 [hp_X]/30 [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.