Helianthus annuus

FDA Drug Profile — Sunflower

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: Provides Potentized homeo-nutritional support for spleen and thymus function.† †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

WARNINGS: Professional Use Only If pregnant or breast-feeding, ask a health professional before use. In case of overdose, get medical help or contact a Poison Control Center right away. If condition worsens, seek medical attention. KEEP OUT OF REACH OF CHILDREN Do not use if tamper evident seal is broken or missing. Store in a cool place after opening