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#
Contacts and useful links#
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
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- CVS Arnica Cream
- Arnica Montana
- PHENOXYETHANOL
- SAFFLOWER OIL
- WATER
- SODIUM POLYACRYLATE (2500000 MW)
- ALCOHOL
- SHEA BUTTER
- COCONUT OIL
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE
- ALOE
- HELIANTHUS ANNUUS SEED WAX
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 51316-995 | 51316-995-25 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| SAFFLOWER OIL | 65UEH262IS | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM POLYACRYLATE (2500000 MW) | 05I15JNI2J | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| ARNICA MONTANA | O80TY208ZW | ACTIB |
| SHEA BUTTER | K49155WL9Y | IACT |
| COCONUT OIL | Q9L0O73W7L | IACT |
| CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE | FJ1H6M2JG9 | IACT |
| ALOE | V5VD430YW9 | IACT |
| HELIANTHUS ANNUUS SEED WAX | 42DG15CHXV | 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 |
|---|---|---|---|---|---|---|
| 471acbcb-03e9-43fd-e063-6394a90a1294 | c72cd6bd-18dc-a711-e053-2a95a90a3087 | 2025-12-29 | Warnings | c72cd6bd-18dc-a711-e053-2a95a90a3087 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
