NETTLE .05 g/mL
URTICA DIOICA POLLEN · INJECTION, SOLUTION · ALK-Abello, Inc.
NETTLE is a injection, solution containing urtica dioica pollen at .05 g/mL, taken percutaneous. Manufactured by ALK-Abello, Inc..
Key Facts
- Brand Name
- NETTLE
- Generic Name
- URTICA DIOICA POLLEN
- NDC Code (Product)
0268-7110- Manufacturer
- ALK-Abello, Inc.
- Strength
- .05 g/mL
- Dosage Form
- INJECTION, SOLUTION
- Route
- PERCUTANEOUS
- Marketing Status
- Application #
- BLA103753
- Marketing Start
- 01/01/1965
Recall History
No Recall HistoryFull Prescribing Information
Indications & Usage
Directions: FOR TOPICAL USE ONLY.
Dosage & Administration
Apply to skin as needed. Under age 2: Consult a doctor.
Warnings
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.
Frequently Asked Questions
What is NETTLE used for?
NETTLE contains URTICA DIOICA POLLEN. It is a injection, solution taken percutaneous. Consult your doctor for specific uses.
Is NETTLE a controlled substance?
NETTLE is not classified as a controlled substance by the DEA.
What is the generic name for NETTLE?
The generic name for NETTLE is URTICA DIOICA POLLEN. There are no other listed brand versions of URTICA DIOICA POLLEN.
What is the NDC code for NETTLE .05 g/mL?
The NDC (National Drug Code) for NETTLE .05 g/mL is 0268-7110, listed by ALK-Abello, Inc..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)