Birch Juniper

FDA Drug Profile — Birch Juniper

Birch Juniper is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Birch Juniper. Available dosage form: liquid.

Drug Details

Generic Name
Birch Juniper
Brand Names
Birch Juniper
Application Number
Sponsor
Uriel Pharmacy Inc
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
JUNIPER BERRY, BETULA PENDULA BARK

Indications and Usage

Directions: FOR ORAL USE ONLY.

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 or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing. SHAKE WELL BEFORE USE. REFRIGERATE AFTER OPENING. BEST WHEN USED WITHIN 30 DAYS OF OPENING.