Arnica Montana 30C

Manufacturer: Schwabe Mexico, S.A. de C.V.
Effective date: 2022-05-20
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: full-release
Hydrated at: 2026-06-01 02:17:27

Label at a glance#

ProductArnica Montana 30C

Active ingredientARNICA MONTANA

Label structure10 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Arnica Montana 30C

Inactive Ingredients

INACTIVE INGREDIENT SECTION

CELLULOSE

CROSCARMELLOSE SODIUM

LACTOSE MONOHYDRATE

MAGNESIUM STEARATE

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Directions: Adults or children over 2 years: Take 3 tablets 1-3 times a day.

Allow to dissolve under tongue.

Indications & Usage

INDICATIONS & USAGE SECTION

Temporarily relieves minor muscle or joint aches and pains from strains, sprains, bruises, backache, over extertion.

Purpose

OTC - PURPOSE SECTION

For the temporary relief of minor muscle or joint aches and pains from strains, sprains, bruises, backache and over exertion.

Warnings

WARNINGS SECTION

Do not use this product for pain for more than 10 days (adult) or 5 days (children) unless directed by a doctor.

When using

OTC - WHEN USING SECTION

When using this product, if pain persists or gets worse, if new symptoms occur, or if redness or swelling is present, consult a doctor because these could be signs of a serious condition.

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Overdosage

OVERDOSAGE SECTION

In case of overdose, seek medical help or contact a Poison Control Center immediately.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

21203574_Arnica montana-30C_05.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68466-1041-2	Arnica Montana 30C	250 in 1 BOTTLE, GLASS	TABLET	250		7
68466-1041-2	Arnica Montana 30C	1 in 1 PACKAGE	TABLET	1		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68466-1041	ARNICA MONTANA 30C (ARNICA MONTANA) TABLET [SCHWABE MEXICO, S.A. DE C.V.]	7	Current NDC, Legacy NDC, 2 package rows	20220521_a4743dcd-dd86-4d56-9d61-3dfb60598076.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Arnica Montana 30C
Arnica Montana
CELLULOSE, MICROCRYSTALLINE
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
CROSCARMELLOSE SODIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
68466-1041	68466-1041-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ARNICA MONTANA	O80TY208ZW	ACTIB
CELLULOSE, MICROCRYSTALLINE	OP1R32D61U	IACT
LACTOSE MONOHYDRATE	EWQ57Q8I5X	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
CROSCARMELLOSE SODIUM	M28OL1HH48	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 30C	ARNICA MONTANA	Schwabe Mexico, S.A. de C.V.	a4743dcd-dd86-4d56-9d61-3dfb60598076	2022-05-20	Warnings	Exact identifier ndc (package): 68466-1041-2 ndc (product): 68466-1041 ndc11 (package): 68466104102 spl id: cd693332-cf97-4139-a5df-0c7164f94730 spl set id: a4743dcd-dd86-4d56-9d61-3dfb60598076

Reported adverse events (FAERS/openFDA)#

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