Lycopodium Berberis 3 [hp_X]/1
Lycopodium Berberis · PELLET · Uriel Pharmacy Inc.
Lycopodium Berberis is a pellet containing lycopodium berberis at 3 [hp_X]/1, taken oral. Manufactured by Uriel Pharmacy Inc..
Key Facts
- Brand Name
- Lycopodium Berberis
- Generic Name
- Lycopodium Berberis
- NDC Code (Product)
48951-6049- Manufacturer
- Uriel Pharmacy Inc.
- Strength
- 3 [hp_X]/1
- Dosage Form
- PELLET
- 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
Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.
Warnings
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.
Frequently Asked Questions
What is Lycopodium Berberis used for?
Lycopodium Berberis contains Lycopodium Berberis. It is a pellet taken oral. Consult your doctor for specific uses.
Is Lycopodium Berberis a controlled substance?
Lycopodium Berberis is not classified as a controlled substance by the DEA.
What is the generic name for Lycopodium Berberis?
The generic name for Lycopodium Berberis is Lycopodium Berberis. There are no other listed brand versions of Lycopodium Berberis.
What is the NDC code for Lycopodium Berberis 3 [hp_X]/1?
The NDC (National Drug Code) for Lycopodium Berberis 3 [hp_X]/1 is 48951-6049, 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)