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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 200 [kp_C]/200 [kp_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
- January 23, 2023
- Manufacturer Document
- Prescribing information, PDF file
- Active ingredient
- Sodium Borate 200 [kp_C]/200 [kp_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
- January 23, 2023
- Manufacturer
- Boiron
- NDC root
- 0220-0876
- Manufacturer Document
- Prescribing information, PDF file
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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 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 further advice.
Uses
If you're dealing with canker sores, this medication can help you find relief. Canker sores are painful 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 discomfort and promote healing.
You can feel reassured knowing that this medication does not have any teratogenic effects (meaning it won't cause birth defects) or nonteratogenic effects. This makes it a safe option for those who may be concerned about potential risks.
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 this routine until your symptoms improve or follow your doctor's specific instructions.
It's important to remember that the medication is meant to be taken under the tongue, which allows it to be absorbed quickly into your system. If you have any questions or concerns about how to use this medication, don't hesitate to reach out to your healthcare provider for guidance.
Warnings and Precautions
It's important to be aware of how to use your medication safely. If your symptoms last more than three days or worsen, you should stop taking the medication and contact your doctor for further guidance.
Currently, there are no specific warnings, precautions, or laboratory tests associated with this medication. However, always stay alert to how you feel while using it and don't hesitate to reach out to your healthcare provider if you have any concerns.
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
It's important to store this product safely by keeping it out of reach of children to prevent any accidental ingestion or misuse. Before using, make sure to 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.
Always handle the product with care to ensure it remains in good condition. Following these simple guidelines 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.
Are there any warnings associated with this medication?
There are no specific warnings provided, but you should stop use and ask a doctor if symptoms persist for more than 3 days or worsen.
What should I do if the pellet dispenser seal is broken?
Do not use the medication if the pellet dispenser seal is broken.
Is this medication safe to use during pregnancy or breastfeeding?
If you are pregnant or breastfeeding, ask a health professional before use.
How should I store this medication?
Keep the medication out of reach of children.
Packaging Info
This section summarizes the homeopathic presentations of Borax (sodium borate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Pellet | 200 [kp_C]/200 [kp_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 200 kp_C. Each pellet contains 0.443 mg of Sodium borate. The inactive ingredients include Sucrose (UNII: C151H8M554) and unspecified form of Lactose (UNII: J2B2A4N98G). The product is characterized by a white color, round shape, and a size of 4 mm. It is administered orally. The product is packaged in a tube containing 200 kp_C pellets, with the item code NDC: 0220-0876-41. The marketing start date is March 3, 1983, and it is classified as an unapproved homeopathic product.
Packaging & NDC
This section summarizes the homeopathic presentations of Borax (sodium borate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Pellet | 200 [kp_C]/200 [kp_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.