Arnicare Arthritis

Manufacturer
Laboratoires Boiron | Boiron Inc. | Boiron
Effective date
2026-07-21
Label type
HUMAN OTC DRUG LABEL
Version
12
Source
daily-update
Hydrated at
2026-07-24 05:10:07

Label at a glance#

ProductArnicare Arthritis
Active ingredientARNICA MONTANA, BENZOIC ACID, BRYONIA ALBA ROOT, MATRICARIA RECUTITA, SOLANUM DULCAMARA TOP, POTASSIUM IODIDE, PULSATILLA VULGARIS, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients** (in each tablet)

Arnica Montana 3C HPUS (0.28 mg)

Benzoicum acidum 6C HPUS (0.28 mg)

Bryonia 6C HPUS (0.28 mg)

Chamomilla 12C HPUS (0.28 mg)

Dulcamara 6C HPUS (0.28 mg)

Kali iodatum 12C HPUS (0.28 mg)

Pulsatilla 3C HPUS (0.28 mg)

Rhododendron chrysanthum 12C HPUS (0.28 mg)

Rhus tox 6C HPUS (0.28 mg)

The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

OTC - PURPOSE SECTION

Purpose*

Arnica Montana 3C HPUS (0.28 mg) ...Relieves joint pain from trauma or overexertion

Benzoicum acidum 6C HPUS (0.28 mg) ...Relieves pain in the wrists

Bryonia 6C HPUS (0.28 mg) ...Relieves joint pain worsened by movement or the slightest touch

Chamomilla 12C HPUS (0.28 mg) ...Relieves sensitivity to pain, tingling and numbing pain

Dulcamara 6C HPUS (0.28 mg) ...Relieves joint pain triggered or worsened by damp weather

Kali iodatum 12C HPUS (0.28 mg) ...Relieves joint and muscle pain worsened at night

Pulsatilla 3C HPUS (0.28 mg) ...Relieves finger joint pain worsened by heat and slow motion

Rhododendron chrysanthum 12C HPUS (0.28 mg) ...Relieves rheumatic pain worsened by dry heat

Rhus toxicodendron 6C HPUS (0.28 mg) ...Relieves joint pain improved by motion and worsened by humidity

INDICATIONS & USAGE SECTION

Uses*

Temporary relieves minor aches and pains associated with arthritis

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 7 days or worsen, new symptoms occur, or if redness or swelling is present. These could be signs of a serious condition.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

Adults 18 years of age and older: At the onset of symptoms, dissolve 2 tablets under the tongue and repeat, if needed, every 15 minutes for 3 more doses. Then, dissolve 2 tablets under the tongue every hour until symptoms improve.

Children under 18 years of age: Ask a doctor.

INACTIVE INGREDIENT SECTION

croscarmellose sodium, lactose, magnesium stearate

SPL UNCLASSIFIED SECTION

do not use if glued carton end flaps are open or if the blister seal is broken

store below 86°F (30°C)

No Known Drug Interactions

Non-Drowsy

Arthritis Pain Relief*

Joint Pain Stiffness*

60 Meltaway Tablets unflavored

100 Meltaway Tablets unflavored

120 Meltaway Tablets unflavored

Made in France

Distributed by Boiron, Inc.

Newtown Square, PA 19073

*CLAIMS BASE ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.

**C, K, CK, and X are homeopathic dilutions: see BoironUSA.com/info for details

OTC - QUESTIONS SECTION

Questions or Comments?

Arnicare.com

BoironUSA.com

Info@boiron.comm

1-800-BOIRON-1
(1-800-264-7661)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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LABELLABEL

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130306969044049GTIN-13: 0306969044049
EAN-13: 0306969044049
GTIN-12: 306969044049
UPC-A: 306969044049
GTIN storage (14 digits): 00306969044049
Arnicare Arthritis 60 ETU.1KES 0225.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0220-9044-04EA - Each0220-9044253d6bd9-9f8e-4da0-bdb0-d01db825702a12021-02-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZW5
BENZOIC ACIDACTIVE INGREDIENT8SKN0B0MIM5
BRYONIA ALBA ROOTACTIVE INGREDIENTT7J046YI2B5
MATRICARIA RECUTITAACTIVE INGREDIENTG0R4UBI2ZZ5
POTASSIUM IODIDEACTIVE INGREDIENT1C4QK22F9J5
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV5
RHODODENDRON AUREUM LEAFACTIVE INGREDIENTIV92NQJ73U5
SOLANUM DULCAMARA TOPACTIVE INGREDIENTKPS1B1162N5
TOXICODENDRON PUBESCENS LEAFACTIVE INGREDIENT6IO182RP7A5
ARNICA MONTANAACTIVE MOIETYO80TY208ZW5
BENZOIC ACIDACTIVE MOIETY8SKN0B0MIM5
BRYONIA ALBA ROOTACTIVE MOIETYT7J046YI2B5
IODIDE IONACTIVE MOIETY09G4I6V86Q5
MATRICARIA RECUTITAACTIVE MOIETYG0R4UBI2ZZ5
PULSATILLA VULGARISACTIVE MOIETYI76KB35JEV5
RHODODENDRON AUREUM LEAFACTIVE MOIETYIV92NQJ73U5
SOLANUM DULCAMARA TOPACTIVE MOIETYKPS1B1162N5
TOXICODENDRON PUBESCENS LEAFACTIVE MOIETY6IO182RP7A5
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH485
LACTOSEINACTIVE INGREDIENTJ2B2A4N98G5
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I305

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-90440220-9044-04, 0220-9044-29, 0220-9044-92

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
112025-03-16full-release2026-06-01 02:32:37

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 12 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / ORAL736 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / ORAL736 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / ORAL736 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / ORAL736 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates

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
Arnicare ArthritisARNICA MONTANA, BENZOIC ACID, BRYONIA ALBA ROOT, MATRICARIA RECUTITA, SOLANUM DULCAMARA TOP, POTASSIUM IODIDE, PULSATILLA VULGARIS, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAFLaboratoires Boironcb02378b-617d-4268-b565-4136e50009f42026-07-21Exact identifier
ndc (package): 0220-9044-29
ndc (package): 0220-9044-04
ndc (package): 0220-9044-92
ndc (product): 0220-9044
ndc11 (package): 00220904429
ndc11 (package): 00220904404
ndc11 (package): 00220904492
spl id: 57227ad0-b164-d600-e063-6294a90a64fa
spl set id: cb02378b-617d-4268-b565-4136e50009f4

Reported adverse events (FAERS/openFDA)#

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