FDA.reportPublic FDA data

Birch Juniper

Manufacturer
Uriel Pharmacy Inc
Effective date
2025-11-18
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:35:13

Label at a glance#

ProductBirch Juniper
Active ingredientJUNIPER BERRY, BETULA PENDULA BARK
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

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

OTC - ACTIVE INGREDIENT SECTION

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

INACTIVE INGREDIENT SECTION

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

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Supports normal kidney function.

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Birch Juniper LiquidBirch Juniper Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-2149-9Birch Juniper240 mL in 1 BOTTLE, GLASSLIQUID2405

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-214948951-2149-9

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
JUNIPER BERRYO84B5194RLACTIB
HONEYY9H1V576FHIACT
BETULA PENDULA BARK40S83Y133CACTIB
SUCROSEC151H8M554IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Birch JuniperBIRCH JUNIPERUriel Pharmacy Inc0fa00042-b326-6d2d-e063-6394a90a236d2025-11-18WarningsExact identifier
ndc (package): 48951-2149-9
ndc (product): 48951-2149
ndc11 (package): 48951214909
spl id: 43e13f9e-f46f-c5ad-e063-6394a90a25d7
spl set id: 0fa00042-b326-6d2d-e063-6394a90a236d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.