Arnicare Cream 0.5oz
- Manufacturer
- Boiron | Boiron Inc.
- Effective date
- 2020-02-25
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 5
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:40:14
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Arnica Montana 1X
INDICATIONS & USAGE SECTION
Temporarily relieves muscle pain and stiffness due to minor injuries, overexertion and falls. Reduces pain, swelling and discoloration from bruises.
OTC - DO NOT USE SECTION
Do not use if you are allergic to Arnica Montana or to any of this product's inactive ingredients. Do not use if the tube seal is broken.
DOSAGE & ADMINISTRATION SECTION
Apply a thin layer of Arnicare Cream to affected area and massage gently as soon as possible after minor injury. Repeat 3 times a day or as needed.
INACTIVE INGREDIENT SECTION
Alcohol, Caprylyl glycol, carbomer, cetyl palmitate, EDTA disodium, glycerin, lauroyl macrogolglycerides, pegoxol-7 stearate, purified water, sodium hydroxide, sorbic acid, 1,2-hexanediol
HOW SUPPLIED SECTION
Tube .5 OZ (14 G)
OTC - PURPOSE SECTION
Arnica Montana 1X ... Trauma, muscle pain & stiffness, swelling from injuries, discoloration from bruising.
OTC - QUESTIONS SECTION
Questions, Comments?
www.Arnicare.com
www.BoironUSA.com
1-800-BOIRON-1
(1-800-264-7661)
Distributed by Boiron Inc.
6 Campus Boulevard
Newtown Square, PA
19073-3267
OTC - ASK DOCTOR SECTION
Ask doctor if condition persists for more than 3 days or worsens.
OTC - STOP USE SECTION
Stop use and ask doctor if condition persists for more than 3 days or worsens.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children
OTC - WHEN USING SECTION
When using this product
- Use only as directed
- Do not bandage lightly or use a heating pad.
SPL UNCLASSIFIED SECTION
- Ideal for Massage
- Soothing
- Unscented
- Paraben-Free
WARNINGS SECTION
For external use only. Avoid contact with eyes, mucous membranes, damaged skin or wounds.
If swallowed, get medical help or contact a Poison Control Center right away.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0220-9021-60 | GM - Gram | 0220-9021 | 81539eba-887c-421c-b1dc-82aa193727c6 | 1 | 2024-05-16 |
| 0220-9021-63 | GM - Gram | 0220-9021 | d381223e-d0c6-4f23-8399-bd7285056915 | 1 | 2021-02-05 |
Products#
Every source-derived product name is available through these pages.
- ARNICARE
- ARNICA MONTANA
- HYDROGENATED PALM/PALM KERNEL OIL PEG-6 ESTERS
- CAPRYLYL GLYCOL
- CARBOMER 934
- CETYL PALMITATE
- EDETATE DISODIUM
- WATER
- SODIUM HYDROXIDE
- SORBIC ACID
- 1,2-HEXANEDIOL
- GLYCERIN
- PEGOXOL 7 STEARATE
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0220-9021 | 0220-9021-68 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HYDROGENATED PALM/PALM KERNEL OIL PEG-6 ESTERS | 8EPU9MJ01K | IACT |
| CAPRYLYL GLYCOL | 00YIU5438U | IACT |
| CARBOMER 934 | Z135WT9208 | IACT |
| CETYL PALMITATE | 5ZA2S6B08X | IACT |
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| SORBIC ACID | X045WJ989B | IACT |
| 1,2-HEXANEDIOL | TR046Y3K1G | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| PEGOXOL 7 STEARATE | 3EW5AXE5X5 | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| ARNICA MONTANA | O80TY208ZW | ACTIB |
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 |
|---|---|---|---|---|---|---|
| ARNICARE | ARNICA MONTANA | Laboratoires Boiron | 542b41dd-f285-4e48-a67b-8e69523b143a | 2026-05-20 | Warnings | 0220-9021-68 0220-9021 00220902168 |
| 69954e24-ab06-5c40-e053-2a91aa0aa254 | 28b3d04b-936f-5c7c-e054-00144ff8d46c | 2018-04-11 | Warnings | 28b3d04b-936f-5c7c-e054-00144ff8d46c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

