Spring Birch Pollen .05 g/mL
Betula occidentalis · SOLUTION · Greer Laboratories, Inc.
Spring Birch Pollen is a solution containing betula occidentalis at .05 g/mL, taken intradermal. Manufactured by Greer Laboratories, Inc..
Key Facts
- Brand Name
- Spring Birch Pollen
- Generic Name
- Betula occidentalis
- NDC Code (Product)
22840-5414- Manufacturer
- Greer Laboratories, Inc.
- Strength
- .05 g/mL
- Dosage Form
- SOLUTION
- Route
- INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
- Marketing Status
- Application #
- BLA101833
- Marketing Start
- 09/15/1981
Recall History
No Recall HistoryFull Prescribing Information
Indications & Usage
Use: For contitutional treatments based on homeopathic and anthroposophic indications or as directed by your physician.
Dosage & Administration
Directions for Use: Place drops under tongue for 30 seconds. Adults 7 drops 3 times a day. Children 2-12 years, 7 drops 3 times a day. Under 2 years, consult your doctor. Use until symptoms are relieved or as directed by your health care provider.
Warnings
Warnings: Consult your health care provider if symptoms persist more than 5 days or worsen.
Frequently Asked Questions
What is Spring Birch Pollen used for?
Spring Birch Pollen contains Betula occidentalis. It is a solution taken intradermal. Consult your doctor for specific uses.
Is Spring Birch Pollen a controlled substance?
Spring Birch Pollen is not classified as a controlled substance by the DEA.
What is the generic name for Spring Birch Pollen?
The generic name for Spring Birch Pollen is Betula occidentalis. There are no other listed brand versions of Betula occidentalis.
What is the NDC code for Spring Birch Pollen .05 g/mL?
The NDC (National Drug Code) for Spring Birch Pollen .05 g/mL is 22840-5414, listed by Greer Laboratories, Inc..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)