Helianthus annuus

FDA Drug Profile — Sunflower

Helianthus annuus is listed in the FDA National Drug Code directory with 5 NDC codes, marketed under brand name including Sunflower. Available dosage form: solution.

Drug Details

Generic Name
Helianthus annuus
Brand Names
Sunflower
Application Number
BLA101833
Sponsor
Greer Laboratories, Inc.
NDC Codes
5
Dosage Forms
SOLUTION
Routes
INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active Ingredients
HELIANTHUS ANNUUS POLLEN

Indications and Usage

Indications & Usage -temporarily protects minor • diapar rash • baby acne -helps prevent and temporarily protects and helps relieve • chapped or cracked skin -helps protect from the drying effects of wind and cold weather -temporarily protects and helps relieve minor skin irritation and itching due to • cradle cap • diaper rash • baby acne • eczema • psoriasis • rashes

Warnings

Warnings Warnings For external use only. -Do not use on • on deep wounds • animal bites • serious burns -Stop use and ask a doctor if • condition worsens • symptoms last more than 7 days or clear up and occur again within a few days -When using this product keep out of eyes. Rinse with water to remove.