FDA.reportPublic FDA data

BMNP-LABEL ARNICA MONTANA 30C

Manufacturer
Total Operations Management LLC DBA:Bestmade Natural Products Micro | BM Private Limited
Effective date
2026-09-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-24 01:00:59

Label at a glance#

ProductBMNP ARNICA MONTANA
Active ingredientARNICA MONTANA WHOLE
Label structure8 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

Keep out of reach of children.

If pregnant or breastfeeding, ask a health professional before use.

Stop use and ask a doctor if symptoms persist or worsen.

If you have severe symptoms, consult a doctor before use.

DOSAGE & ADMINISTRATION SECTION

Use as directed.

Take with water, 3-4 times daily. Ages 12 and older: 2 pellets. Ages 3 to 11: 1 pellet. Ages below 3: consult your doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If pregnant or breastfeeding, ask a health professional before use.

Stop use and ask a doctor if symptoms persist or worsen.

If you have severe symptoms, consult a doctor before use.

INDICATIONS & USAGE SECTION

Helps temporarily relieve: discomfort associated with strong aches, including back and shoulder pain, bruising, muscle soreness, overexertion, injuries, muscle strains, and swelling.

OTC - PURPOSE SECTION

Arnica Montana 30C (HPUS)......bruising, muscle soreness, minor injury pain

"HPUS" is the Homeopathic Pharmacopoeia of the United States.

OTC - ACTIVE INGREDIENT SECTION

ARNICA MONTANA 30C

INACTIVE INGREDIENT SECTION

Sucrose, PVP K 30, Magnesium Stearate, Aerosil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package 1

Arnica Mont 30CArnica Mont 30C

Package 2

Arnica MontanaArnica Montana

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codefastremedypicker.com/-_Arnica Montana 30C.jpg

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82969-523482969-5234-1, 82969-5234-2

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
NameUNIIKind
ARNICA MONTANA WHOLEO80TY208ZWACTIB
SUCROSEC151H8M554IACT
MAGNESIUM STEARATE70097M6I30IACT
POVIDONE K30U725QWY32XIACT
SILICON DIOXIDEETJ7Z6XBU4IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-09-01daily-update2026-09-03 03:01:26

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
5a6b2e38-c99c-83de-e063-6394a90a56f85a6b2d06-3d53-874e-e063-6394a90af2b82026-09-01WarningsExact identifier
spl set id: 5a6b2d06-3d53-874e-e063-6394a90af2b8

Reported adverse events (FAERS/openFDA)#

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