DOSAGE & ADMINISTRATION SECTION
How to Use
Take with water 3-4 times a day. Ages 12 or older, 5 Pellets, Ages 12-2, 3 Pellets, Ages below 2, consult your Doctor.
Bestmade Natural Products Arnica Montana
- Manufacturer
- Bestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro
- Effective date
- 2025-03-07
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:32:53
Label at a glance#
ProductBestmade Natural Products Arnica Montana
Active ingredientARNICA MONTANA
Label structure8 sections
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Uses
Temporarily relieves occasional shoulder, neck, and back aches. It also temporarily relieves occasional bruising, muscle soreness from overexertion or injury, strains, sprains, and swelling.*
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE, NOT FDA EVALUATED. This product is not intended to diagnose, treat, cure, or prevent any disease.
OTC - PURPOSE SECTION
Uses
Temporarily relieves occasional shoulder, neck, and back aches. It also temporarily relieves occasional bruising, muscle soreness from overexertion or injury, strains, sprains, and swelling.*
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE, NOT FDA EVALUATED. This product is not intended to diagnose, treat, cure, or prevent any disease.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Arnica Montana (Wolf's Bane) [HPUS] 30C potency
INACTIVE INGREDIENT SECTION
Ingredients
Inactive: Sucrose/Lactose Pellets base to Preserve Remedy
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Warnings and Storage:
Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.
WARNINGS SECTION
Warnings and Storage:
Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE, NOT FDA EVALUATED. This product is not intended to diagnose, treat, cure, or prevent any disease.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Entire package label
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82969-5014-1 | Bestmade Natural Products Arnica Montana | 30 [hp_C] in 1 BOTTLE, GLASS | TABLET, SOLUBLE | 30 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 82969-5014 | BESTMADE NATURAL PRODUCTS ARNICA MONTANA (ARNICA MONTANA) TABLET, SOLUBLE [BESTMADE NATURAL PRODUCTS] | 2 | Current NDC, 1 package rows | 20250327_29a17477-5178-0771-e063-6294a90ae129.zip |
Products#
Every source-derived product name is available through these pages.
- Bestmade Natural Products Arnica Montana
- Arnica Montana
- SUCROSE
- LACTOSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 82969-5014 | 82969-5014-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ARNICA MONTANA | O80TY208ZW | ACTIB |
| SUCROSE | C151H8M554 | IACT |
| LACTOSE | J2B2A4N98G | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Bestmade Natural Products Arnica Montana | ARNICA MONTANA | Bestmade Natural Products | 29a17477-5178-0771-e063-6294a90ae129 | 2025-03-07 | Warnings | 82969-5014-1 82969-5014 82969501401 2fbf280b-daef-f774-e063-6294a90afef9 29a17477-5178-0771-e063-6294a90ae129 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.