Urtica dioica

FDA Drug Profile — Nettle, Nettle Pollen

Urtica dioica is listed in the FDA National Drug Code directory with 5 NDC codes, marketed under brand names including Nettle, Nettle Pollen. Available dosage forms: solution, injection.

Drug Details

Generic Name
Urtica dioica
Brand Names
Nettle, Nettle Pollen
Application Number
BLA101833
Sponsor
Greer Laboratories, Inc.
NDC Codes
5
Dosage Forms
SOLUTION, INJECTION
Routes
INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS, CUTANEOUS
Active Ingredients
URTICA DIOICA POLLEN

Indications and Usage

USES: For temporary relief of skin irritation, dry cough, eczema, and fever.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

WARNINGS: Sore Throat Warning Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult physician promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by physician. If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.