Dr. Hendel Arnica Montana 3X, 6X, 12X, 30X, 200X Tablet

Manufacturer: MediNatura Inc
Effective date: 2022-08-18
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 02:18:02

Label at a glance#

ProductArnica Montana 3X, 6X, 12X, 30X, 200X

Active ingredientARNICA MONTANA ROOT

Label structure8 sections

Indications and uses

For the temporary relief of: • Symptoms of bruising • Pain

Dosage and administration

Dosage: Adults 18 and over : 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician.

Label contents#

Full prescribing information#

WARNINGS

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or

worsen, a health professional should be consulted. Do not use if sensitivity to Hendel Arnica montana 3X, 6X, 12X, 30X, 200X or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS

OTC - PURPOSE SECTION

• Symptoms of bruising

• Pain

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Arnica Montana 3X, 6X, 12X, 30X, 200X

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Lactose, Magnesium stearate

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Dosage: Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician.

USES

INDICATIONS & USAGE SECTION

For the temporary relief of:

• Symptoms of bruising

• Pain

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Arnica Montana

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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62795-1112-2	Arnica Montana 3X, 6X, 12X, 30X, 200X	100 in 1 BOTTLE	TABLET	100		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62795-1112	ARNICA MONTANA 3X, 6X, 12X, 30X, 200X (ARNICA MONTANA ROOT) TABLET [MEDINATURA INC]	3	Current NDC, Legacy NDC, 1 package rows	20220820_826f5ce1-b149-449f-b4dd-229e9ab4e40a.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
62795-1112-2	EA - Each	62795-1112	0c926107-75e2-4b4b-9ca1-6eb93c7324f8	1	2017-04-05

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Arnica Montana 3X, 6X, 12X, 30X, 200X
ARNICA MONTANA ROOT
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62795-1112	62795-1112-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ARNICA MONTANA ROOT	MUE8Y11327	ACTIB
LACTOSE MONOHYDRATE	EWQ57Q8I5X	IACT
MAGNESIUM STEARATE	70097M6I30	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Arnica Montana 3X, 6X, 12X, 30X, 200X	ARNICA MONTANA ROOT	MediNatura Inc	826f5ce1-b149-449f-b4dd-229e9ab4e40a	2022-08-18	Warnings	Exact identifier ndc (package): 62795-1112-2 ndc (product): 62795-1112 ndc11 (package): 62795111202 spl id: 0a6b0e83-5280-4742-b415-a8404c2ec0e5 spl set id: 826f5ce1-b149-449f-b4dd-229e9ab4e40a

Reported adverse events (FAERS/openFDA)#

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