CVS Arnica Cream

Manufacturer
CVS Health
Effective date
2024-12-09
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:46:55

Label at a glance#

ProductCVS Arnica Cream
Active ingredientARNICA MONTANA
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Arnica Montana 1X HPUS-7%

OTC - PURPOSE SECTION

Trauma, Muscle Pain and stiffness, swelling from injuries, discoloration from bruising.

The letters HPUS indicate that this ingredient is officially included in the Homeopathic Pharmacopoeia of the United States.

INDICATIONS & USAGE SECTION

temporarily relieves muscle pain and stiffness due to minor injuries, overexertion, and falls

reduces pain, swelling and discoloration from bruises

WARNINGS SECTION

For external use only

Avoid contact with eyes, mucous membrane, damaged skin, or wounds.

OTC - DO NOT USE SECTION

If you are allergic to Arnica montana or to any of this product's inactive ingredient.

OTC - WHEN USING SECTION

Use only as directed.

Do not bandage tightly or use a heating pad.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Apply a thin layer of Arnica Cream to the affected area and massage gently as soon as possible after a minor injury, repeat 3 times a day or as needed.

OTHER SAFETY INFORMATION

Store at 20-25 C (68-77 F)

Do not use if the tube seal is broken

INACTIVE INGREDIENT SECTION

Alcohol, Aloe Oil, Caprylic/Capric Triglycerides, Coconut oil, Helianthus Annus seed wax, and Sodium polyacrylate, Phenoxyethanol, Purified water, safflower oil, Shea butter.

OTC - QUESTIONS SECTION

1-800-746-7287

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51316-995CVS ARNICA CREAM (ARNICA MONTANA) CREAM [CVS HEALTH]5Legacy NDC20241213_c72cd6bd-18dc-a711-e053-2a95a90a3087.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51316-99551316-995-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
471acbcb-03e9-43fd-e063-6394a90a1294c72cd6bd-18dc-a711-e053-2a95a90a30872025-12-29WarningsExact identifier
spl set id: c72cd6bd-18dc-a711-e053-2a95a90a3087

Reported adverse events (FAERS/openFDA)#

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