FDA.reportPublic FDA data

Birch Juniper Rejuvenation Syrup

Manufacturer
Uriel Pharmacy Inc.
Effective date
2021-09-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:34:47

Label at a glance#

ProductBirch Juniper Rejuvenation Syrup
Active ingredientBETULA PENDULA BARK, JUNIPER BERRY
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

Ingredients: Birch leaf extract, Juniper berry extract

INACTIVE INGREDIENT SECTION

Ingredients: Distilled water, Sucanat, Honey, Citric acid

OTC - PURPOSE SECTION

Use: Supports normal kidney function.*

*This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: 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.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Birch Juniper Rejuvenation SyrupBirch Juniper Rejuvenation Syrup

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
48951-214248951-2142-9

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
BETULA PENDULA BARK40S83Y133CACTIB
HONEYY9H1V576FHIACT
JUNIPER BERRYO84B5194RLACTIB
SUCROSEC151H8M554IACT
WATER059QF0KO0RIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT

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
26ce4028-6b46-70e7-e063-6394a90a5be9cd117e2d-b9f2-4911-e053-2995a90a7af92024-11-13WarningsExact identifier
spl set id: cd117e2d-b9f2-4911-e053-2995a90a7af9

Reported adverse events (FAERS/openFDA)#

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