Lycopodium Berberis
Lycopodium Berberis is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Lycopodium Berberis. Available dosage form: pellet.
Drug Details
- Generic Name
- Lycopodium Berberis
- Brand Names
- Lycopodium Berberis
- Application Number
- Sponsor
- Uriel Pharmacy Inc.
- NDC Codes
- 1
- Dosage Forms
- PELLET
- Routes
- ORAL
- Active Ingredients
- MILK THISTLE, BERBERIS VULGARIS ROOT BARK, LYCOPODIUM CLAVATUM SPORE, CHELIDONIUM MAJUS ROOT, TURMERIC, FRAGARIA VESCA WHOLE, VITIS VINIFERA LEAF, SULFIDE ION, CALOMEL
Indications and Usage
Directions: FOR ORAL USE ONLY.
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.