Walgreens Arnica Pain Relieving Gel Arnica Montana1X HPUS 7%

Manufacturer
WALGREENS CO.
Effective date
2022-04-12
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:17:19

Label at a glance#

ProductArnica Montana
Active ingredientARNICA MONTANA
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Arnica montana 1X HPUS 7%

INACTIVE INGREDIENT SECTION

alcohol, carbomer, purified water, sodium hydroxide

DOSAGE & ADMINISTRATION SECTION

Apply a thin layer of gel to affected area and massage gently as soon as possible after minor injury. Repeat 3 times a day or as needed.

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

When using this product avoid contact with eyes, mucous membranes, damaged skin, or wounds.

Do not use if you are allergic to Arnica montana or to any of this product’s inactive ingredients.

When using this product use only as directed, do not bandage tightly or use a heating pad.

Stop use and ask a doctor if condition persists for more than 3 days or worsens.

Keep out of reach of children.

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

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.

OTC - PURPOSE SECTION

Trauma, muscle pain, and stiffness, swelling from injuries, discoloration from bruising

OTHER SAFETY INFORMATION

Do not use if glued carton end flaps are open or if the tube seal is broken.

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CT515026CT515026LB515026LB515026

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-5150-26Arnica Montana74 g in 1 PACKAGEGEL744

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-5150ARNICA MONTANA GEL [WALGREENS CO.]4Current NDC, Legacy NDC, 1 package rows20220413_995d7e44-83a4-0d31-e053-2a95a90a2acb.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0363-5150-26GM - Gram0363-51505129f932-4257-488f-918c-ff84747b648f12022-06-06

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-51500363-5150-26

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
Arnica MontanaARNICA MONTANAWALGREENS CO.995d7e44-83a4-0d31-e053-2a95a90a2acb2022-04-12WarningsExact identifier
ndc (package): 0363-5150-26
ndc (product): 0363-5150
ndc11 (package): 00363515026
spl id: dc793108-68db-1323-e053-2995a90af598
spl set id: 995d7e44-83a4-0d31-e053-2a95a90a2acb

Reported adverse events (FAERS/openFDA)#

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