Walgreens Arnica Spray
- Manufacturer
- Walgreens
- Effective date
- 2022-11-30
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:18:44
Label at a glance#
ProductWalgreens Arnica
Active ingredientARNICA MONTANA
Label structure8 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Arnica montana 1 X HPUS 7%
OTC - PURPOSE SECTION
Trauma, muscle pain and stiffness, swelling from injuries, discoloration from bruising
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
OTC - DO NOT USE SECTION
Do not use if you are allergic to Arnica montana or to any of this product's inactive ingredients.
Extremely Flammable
do not use near heat or flame or while smoking
avoid long term storage above 104°F (40°C)
do not puncture or incinerate. Contents under pressure
do not store at temperatures above 120°F (49°C)
OTC - WHEN USING SECTION
When using this product
Use only as directed
Avoid spraying on face
Avoid inhalation of spray
Do not bandage or apply local heat (such as heating pads) or a medicated patch to area of use
OTC - ASK DOCTOR SECTION
Stop use and ask a doctor if
irritation develops
condition persist for more than 3 days or worsens
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast feeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
If swallowed, get medical help or contact a poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Directions:
adults and children over 12 years:
Apply to affected area and massage until thoroughly absorbed into skin.
Repeat 3 times a day or as needed.
Children 12 years or younger: ask a doctor
INACTIVE INGREDIENT SECTION
Alcohol, Carbomer, phenoxyethanol, sodium hydroxide, tetrafluoroethene, water
OTC - QUESTIONS SECTION
Questions or comments ? 1-800-925-4733
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0363-3034-07 | Walgreens Arnica | 113 g in 1 BOTTLE, SPRAY | AEROSOL, SPRAY | 113 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Walgreens Arnica
- Arnica Montana 7%
- ARNICA MONTANA
- ISOPROPYL ALCOHOL
- SODIUM HYDROXIDE
- NORFLURANE
- WATER
- CARBOMER 940
- PHENOXYETHANOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0363-3034 | 0363-3034-07 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ARNICA MONTANA | O80TY208ZW | ACTIB |
| ISOPROPYL ALCOHOL | ND2M416302 | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| NORFLURANE | DH9E53K1Y8 | IACT |
| WATER | 059QF0KO0R | IACT |
| CARBOMER 940 | 4Q93RCW27E | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | 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 |
|---|---|---|---|---|---|---|
| Walgreens Arnica | ARNICA MONTANA 7% | Walgreens | ce169ac8-f93f-daed-e053-2995a90aa743 | 2022-11-30 | Warnings | 0363-3034-07 0363-3034 00363303407 eea1704f-9bb8-9f9e-e053-2a95a90a1d57 ce169ac8-f93f-daed-e053-2995a90aa743 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.