American Elm

FDA Drug Profile — ULMUS AMERICANA POLLEN

American Elm is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including ULMUS AMERICANA POLLEN. Available dosage form: injection, solution.

Drug Details

Generic Name
American Elm
Brand Names
ULMUS AMERICANA POLLEN
Application Number
BLA103753
Sponsor
ALK-Abello, Inc.
NDC Codes
1
Dosage Forms
INJECTION, SOLUTION
Routes
PERCUTANEOUS
Active Ingredients
ULMUS AMERICANA POLLEN

Indications and Usage

INDICATIONS Provides factors that mitigate hypersensitivity to broadleaf and needle-bearing trees.† †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