Berberis Oxalis 2 [hp_X]/mL
Berberis Oxalis · LIQUID · Uriel Pharmacy Inc.
Berberis Oxalis is a liquid containing berberis oxalis at 2 [hp_X]/mL, taken oral. Manufactured by Uriel Pharmacy Inc..
Key Facts
- Brand Name
- Berberis Oxalis
- Generic Name
- Berberis Oxalis
- NDC Code (Product)
48951-2161- Manufacturer
- Uriel Pharmacy Inc.
- Strength
- 2 [hp_X]/mL
- Dosage Form
- LIQUID
- Route
- ORAL
- Marketing Status
- Marketing Start
- 09/01/2009
Recall History
No Recall HistoryFull Prescribing Information
Indications & Usage
Directions: FOR ORAL USE ONLY.
Dosage & Administration
Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.
Warnings
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.
Frequently Asked Questions
What is Berberis Oxalis used for?
Berberis Oxalis contains Berberis Oxalis. It is a liquid taken oral. Consult your doctor for specific uses.
Is Berberis Oxalis a controlled substance?
Berberis Oxalis is not classified as a controlled substance by the DEA.
What is the generic name for Berberis Oxalis?
The generic name for Berberis Oxalis is Berberis Oxalis. There are no other listed brand versions of Berberis Oxalis.
What is the NDC code for Berberis Oxalis 2 [hp_X]/mL?
The NDC (National Drug Code) for Berberis Oxalis 2 [hp_X]/mL is 48951-2161, listed by Uriel Pharmacy Inc..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)