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Uva Ursi
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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
- Arctostaphylos Uva-Ursi Leaf 6 [hp_C]/6 [hp_C]
- Other brand names
- Dosage form
- Pellet
- Route
- Oral
- Prescription status
- Homeopathic
- Marketed in the U.S.
- Since 1983
- Label revision date
- November 15, 2023
- Manufacturer Document
- Prescribing information, PDF file
- Active ingredient
- Arctostaphylos Uva-Ursi Leaf 6 [hp_C]/6 [hp_C]
- Other brand names
- 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 15, 2023
- Manufacturer
- Boiron
- NDC root
- 0220-5161
- Manufacturer Document
- Prescribing information, PDF file
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Drug Overview
It seems that the information provided does not include specific details about the drug's name, general description, or its mechanism of action. However, based on the context, it appears that the drug may be related to addressing abdominal cramps during urination.
If you are experiencing abdominal cramps while urinating, it is important to consult with a healthcare professional for proper evaluation and treatment options. They can provide you with the necessary information about medications that may help alleviate your symptoms and improve your comfort.
Uses
If you're experiencing abdominal cramps during urination, this medication may be used to help alleviate that discomfort. It's important to note that there are no known teratogenic effects (which means it doesn't cause birth defects) associated with this medication. 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 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. This method helps ensure that the medication is absorbed effectively into your system.
Warnings and Precautions
It's important to be aware of certain precautions while 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.
Currently, there are no specific warnings or emergency instructions provided for this medication. However, always stay alert to how you feel and seek medical advice 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 action 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. When handling the device, ensure that you do not use it if the seal on the pellet dispenser is broken, as this could compromise its safety and effectiveness.
Always check the packaging before use to ensure everything is intact. 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 should I do if I experience abdominal cramps during urination?
You can dissolve 5 pellets under your tongue 3 times a day at the onset of symptoms until they are relieved or as directed by a doctor.
Are there any teratogenic effects associated with this drug?
No teratogenic effects have been mentioned for this drug.
What should I do if my symptoms persist or worsen?
You should stop using the drug and ask a doctor if symptoms persist for more than 3 days or worsen.
Is this drug safe for children?
Yes, the same dosage instructions apply to both adults and children.
What precautions should I take when using this drug?
Keep the drug out of reach of children and do not use it if the pellet dispenser seal is broken.
Should I consult a doctor if I am pregnant or breastfeeding?
Yes, you should ask a health professional before use if you are pregnant or breastfeeding.
Packaging Info
This section summarizes the homeopathic presentations of Uva Ursi (arctostaphylos uva-ursi leaf). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Pellet | 6 [hp_C]/6 [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:
UVA URSI is a homeopathic medicinal product containing Arctostaphylos uva-ursi leaf as the active ingredient, with a strength of 6 hp_C. Each pellet contains 0.443 mg of the active ingredient. The product is formulated with inactive ingredients including sucrose (UNII: C151H8M554) and unspecified form of lactose (UNII: J2B2A4N98G).
UVA URSI pellets are characterized by their white color, round shape, and a size of 4 mm. The product is packaged in a tube containing 6 pellets, classified as Type 0: Not a Combination Product, with the item code NDC: 0220-5161-41. The marketing start date for this product is March 3, 1983. The labeler and registrant for UVA URSI is Boiron, Inc. (Labeler Code: 282560473, Registrant Code: 014892269).
Packaging & NDC
This section summarizes the homeopathic presentations of Uva Ursi (arctostaphylos uva-ursi leaf). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Pellet | 6 [hp_C]/6 [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 Uva Ursi. It includes information on ingredients, suggested use, and labeling language. This product is not FDA-approved.