Drugplain

American Hazelnut Pollen .1 g/mL

Corylus americana · SOLUTION · Greer Laboratories, Inc.

No Recall History
Plain English

American Hazelnut Pollen is a solution containing corylus americana at .1 g/mL, taken intradermal. Manufactured by Greer Laboratories, Inc..

Key Facts

Brand Name
American Hazelnut Pollen
Generic Name
Corylus americana
NDC Code (Product)
22840-2413
Manufacturer
Greer Laboratories, Inc.
Strength
.1 g/mL
Dosage Form
SOLUTION
Route
INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Marketing Status
Application #
BLA101833
Marketing Start
09/15/1981

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

INDICATIONS Low energy, congestion, spasms.

Dosage & Administration

SUGGESTED DOSAGE One dropper full twice daily.

Warnings

Warnings Use only if cap seal is unbroken. If pregnant or breastfeeding, ask a healthcare professional before use. Keep this and all medication out of the reach of children.

Frequently Asked Questions

What is American Hazelnut Pollen used for?

American Hazelnut Pollen contains Corylus americana. It is a solution taken intradermal. Consult your doctor for specific uses.

Is American Hazelnut Pollen a controlled substance?

American Hazelnut Pollen is not classified as a controlled substance by the DEA.

What is the generic name for American Hazelnut Pollen?

The generic name for American Hazelnut Pollen is Corylus americana. There are 2 other brand versions of Corylus americana.

What is the NDC code for American Hazelnut Pollen .1 g/mL?

The NDC (National Drug Code) for American Hazelnut Pollen .1 g/mL is 22840-2413, listed by Greer Laboratories, Inc..

Product NDC

22840-2413

Package NDC

22840-2413-2

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)