FDA.reportPublic FDA data

Juniperus Eucalyptus

Manufacturer
Uriel Pharmacy, Inc.
Effective date
2023-09-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:22:14

Label at a glance#

ProductJuniperus Eucalyptus
Active ingredientLARIX DECIDUA RESIN, CAMPHOR (NATURAL), ACORUS CALAMUS ROOT, BERBERIS VULGARIS ROOT BARK, C12-17 ALKANE, SOLIDAGO VIRGAUREA FLOWERING TOP
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take 2 capsules in the morning on an empty stomach. In acute cases, take 2 more capsules at bedtime. Ages 12 and older: 2 capsules. Ages 2-11: 1 capsule. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: 100gm contains: 30gm Berberis (Barberry) 1X, 10gm Calamus (Sweet flag) 3X, 10gm Camphora (Camphor) 3X, 10gm Iris 3X, 10gm Resina laricis (Larch resin) 3X, 10gm Solidago (Goldenrod) 3X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Vegetable capsules, Organic flax seed oil, Castor oil, Cod liver oil, Eucalyptus oil, Dwarf pine oil, Anise oil, Fennel oil, Juniper oil

OTC - PURPOSE SECTION

Use: Temporary relief of cold symptoms.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

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.

KEEP REFRIGERATED

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

Juniperus Eucalyptus Oil CapsulesJuniperus Eucalyptus Oil Capsules

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-6082-7Juniperus Eucalyptus90 in 1 BOTTLE, GLASSCAPSULE, LIQUID FILLED901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-6082JUNIPERUS EUCALYPTUS CAPSULE, LIQUID FILLED [URIEL PHARMACY, INC.]11 package rows20230914_05182654-5b50-c78a-e063-6394a90abfab.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-608248951-6082-7

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
PINE NEEDLE OIL (PINUS MUGO)6KF1RLN1CIIACT
ANISE OIL6Y89129C8HIACT
JUNIPERUS OXYCEDRUS LEAF OILYNW2QPG8YKIACT
LARIX DECIDUA RESINAD8LJ73GQFACTIB
CAMPHOR (NATURAL)N20HL7Q941ACTIB
ACORUS CALAMUS ROOTXY1K7KIQ0FACTIB
LINSEED OIL84XB4DV00WIACT
POWDERED CELLULOSESMD1X3XO9MIACT
BERBERIS VULGARIS ROOT BARK1TH8Q20J0UACTIB
CASTOR OILD5340Y2I9GIACT
COD LIVER OILBBL281NWFGIACT
EUCALYPTUS OIL2R04ONI662IACT
FENNEL OIL59AAO5F6HTIACT
C12-17 ALKANEFW7807707BACTIB
SOLIDAGO VIRGAUREA FLOWERING TOP5405K23S50ACTIB

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
05182654-5b51-c78a-e063-6394a90abfab05182654-5b50-c78a-e063-6394a90abfab2023-09-11WarningsExact identifier
spl id: 05182654-5b51-c78a-e063-6394a90abfab
spl set id: 05182654-5b50-c78a-e063-6394a90abfab

Reported adverse events (FAERS/openFDA)#

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