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#

ProductARNICARE
Active ingredientARNICA MONTANA
Label structure15 sections

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

boxboxboxbox

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0220-9021-60GM - Gram0220-902181539eba-887c-421c-b1dc-82aa193727c612024-05-16
0220-9021-63GM - Gram0220-9021d381223e-d0c6-4f23-8399-bd728505691512021-02-05

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-90210220-9021-68

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ARNICAREARNICA MONTANALaboratoires Boiron542b41dd-f285-4e48-a67b-8e69523b143a2026-05-20WarningsExact identifier
ndc (package): 0220-9021-68
ndc (product): 0220-9021
ndc11 (package): 00220902168
69954e24-ab06-5c40-e053-2a91aa0aa25428b3d04b-936f-5c7c-e054-00144ff8d46c2018-04-11WarningsExact identifier
spl set id: 28b3d04b-936f-5c7c-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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