Birch Juniper by Uriel Pharmacy Inc BIRCH JUNIPER liquid

Birch Juniper by

Drug Labeling and Warnings

Birch Juniper by is a Homeopathic medication manufactured, distributed, or labeled by Uriel Pharmacy Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION

Take 2 times daily. Ages 12 and older: 1-2 teaspoons. Ages 2-11: 1/2 teaspoon. Under age 2: Consult a doctor.

ACTIVE INGREDIENT

Active Ingredients: 1gm contains: 400mg Betula (Birch Leaf) 1X, 300mg Juniperus (Juniper berry) 1X

INACTIVE INGREDIENT

Inactive Ingredients: Distilled water, Sucanat, Honey, Citric acid

Prepared using rhythmical processes.

PURPOSE

Use: Supports normal kidney function.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

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
90 DAYS OF OPENING.

QUESTIONS

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
shopuriel.com Lot:

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BIRCH JUNIPER 
birch juniper liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-2149
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
JUNIPER BERRY (UNII: O84B5194RL) (JUNIPER BERRY - UNII:O84B5194RL)	JUNIPER BERRY	1 [hp_X]  in 1 mL
BETULA PENDULA BARK (UNII: 40S83Y133C) (BETULA PENDULA BARK - UNII:40S83Y133C)	BETULA PENDULA BARK	1 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HONEY (UNII: Y9H1V576FH)
SUCROSE (UNII: C151H8M554)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-2149-9	240 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	11/03/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		11/03/2021

Labeler - Uriel Pharmacy Inc (043471163)

Establishment
Name	Address	ID/FEI	Business Operations
Uriel Pharmacy Inc		043471163	manufacture(48951-2149)