Beech
Beech is listed in the FDA National Drug Code directory with 3 NDC codes, marketed under brand name including FAGUS GRANDIFOLIA POLLEN. Available dosage form: injection, solution.
Drug Details
- Generic Name
- Beech
- Brand Names
- FAGUS GRANDIFOLIA POLLEN
- Application Number
- BLA103753
- Sponsor
- ALK-Abello, Inc.
- NDC Codes
- 3
- Dosage Forms
- INJECTION, SOLUTION
- Routes
- SUBCUTANEOUS, PERCUTANEOUS
- Active Ingredients
- FAGUS GRANDIFOLIA POLLEN
Indications and Usage
Uses: For temporary relief of minor: irritability* headache* muscle tension* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Warnings
Warnings: If pregnant or breastfeeding , ask a health professional before use. Do not use if clear seal over the cap is broken or missing. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if irritability, headache, muscle tension, or other symptoms do not improve within 7 days or are accompanied by fever.