Drugplain

Nettle .025 g/mL

Urtica dioica · SOLUTION · Greer Laboratories, Inc.

No Recall History
Plain English

Nettle is a solution containing urtica dioica at .025 g/mL, taken intradermal. Manufactured by Greer Laboratories, Inc..

Key Facts

Brand Name
Nettle
Generic Name
Urtica dioica
NDC Code (Product)
22840-5317
Manufacturer
Greer Laboratories, Inc.
Strength
.025 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

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. It is a solution taken intradermal. 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. There are 6 other brand versions of Urtica dioica.

What is the NDC code for Nettle .025 g/mL?

The NDC (National Drug Code) for Nettle .025 g/mL is 22840-5317, listed by Greer Laboratories, Inc..

Product NDC

22840-5317

Package NDC

22840-5317-2

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

Data from openFDA · Public domain (CC0 1.0)