Arnica e pl. tota 6

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-04-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:59:52

Label at a glance#

ProductArnica e pl. tota 6
Active ingredientARNICA MONTANA
Label structure2 sections

Label contents#

Full prescribing information#

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.

REFRIGERATE AFTER OPENING.
BEST WHEN USED WITHIN 90 DAYS OF OPENING.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ArnicaEpl.Tota6xLiquidArnicaEpl.Tota6xLiquid

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-830848951-8308-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ARNICA MONTANAO80TY208ZWACTIB

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
c70507f3-b21f-66e7-e053-2a95a90adeae3fcb4594-cce4-46ee-e054-00144ff88e882021-07-13WarningsExact identifier
spl set id: 3fcb4594-cce4-46ee-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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