FDA.reportPublic FDA data

Berberis Larix

Manufacturer
Uriel Pharmacy Inc
Effective date
2024-12-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:29:44

Label at a glance#

ProductBerberis Larix
Active ingredientACHILLEA MILLEFOLIUM, BERBERIS VULGARIS ROOT BARK, EQUISETUM ARVENSE TOP, LYTTA VESICATORIA, APIS MELLIFERA, LARIX DECIDUA RESIN, SUS SCROFA URINARY BLADDER, FERROUS DISULFIDE
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Achillea (Yarrow) 3X, Berberis (Barberry) 3X, Equisetum (Common horsetail) 3X, Cantharis (Spanish fly) 6X, Apis (Honeybee) 8X, Pyrite (Nat. Iron disulfide) 8X, Resina laricis (Larch resin) 8X, Vesica urinaria (Bovine urinary bladder) 8X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic sucrose, Lactose

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Temporary relief of bladder irritation.

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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Contains traces of lactose. 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.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Berberis Larix PelletsBerberis Larix Pellets

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-2157-22026-01-29C16284748780-149896155-a57d-586f-e063-e6dba90add90Berberis Larix

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-2157-2Berberis Larix1350 in 1 BOTTLE, GLASSPELLET13501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-2157BERBERIS LARIX PELLET [URIEL PHARMACY INC]11 package rows20241222_298d74fa-3029-a224-e063-6294a90a81d5.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-215748951-2157-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
ACHILLEA MILLEFOLIUM2FXJ6SW4PKACTIB
BERBERIS VULGARIS ROOT BARK1TH8Q20J0UACTIB
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB
LYTTA VESICATORIA3Q034RO3BTACTIB
APIS MELLIFERA7S82P3R43ZACTIB
LARIX DECIDUA RESINAD8LJ73GQFACTIB
SUS SCROFA URINARY BLADDER3G7U72W8DAACTIB
FERROUS DISULFIDE132N09W4PRACTIB
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT

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
298d8c06-7973-7cc0-e063-6394a90a3e43298d74fa-3029-a224-e063-6294a90a81d52024-12-17WarningsExact identifier
spl id: 298d8c06-7973-7cc0-e063-6394a90a3e43
spl set id: 298d74fa-3029-a224-e063-6294a90a81d5

Reported adverse events (FAERS/openFDA)#

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