ARNICA

Manufacturer
ONA STICK USA LLC | Abinter Labs LLC
Effective date
2022-03-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:17:10

Label at a glance#

ProductARNICA
Active ingredientARNICA MONTANA FLOWER, CALENDULA OFFICINALIS FLOWER, HAMAMELIS VIRGINIANA LEAF, CHAMOMILE
Label structure10 sections

Indications and uses

Temporarily relieves minor pain, discomfort, bumps and bruises due to minor injuries, falls, trauma and overexertion.

Dosage and administration

Apply a thin layer to affected areas, massaging onto skin. Repeat as needed. If heat or ice are applied to skin, wait 10 minutes before applying product.

Storage and handling

Keep cap firmly in place between uses. Store at room temperature in a dry place. Retain this tip card for full Drug Facts.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredientsPurpose
Arnica montana (Arnica), 1X, 2.5%
Calendula officinalis (Calendula), 1X, 1.8%
Hamamelis virginiana (Witch Hazel), 1X, 2.5%
Matricaria chamomilla (Chamomile), 1X, 2.0%
For relief of minor pain, discomfort, bumps & bruises

UsesAs a homeopathic medicine, these "Uses" have not been evaluated by the Food & Drug Administration.

INDICATIONS & USAGE SECTION

Temporarily relieves minor pain, discomfort, bumps and bruises due to minor injuries, falls, trauma and overexertion.

Warnings

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use if you are allergic to any of the active ingredients or inactive ingredients in this product.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes and mouth
  • do not use on wounds or irritated or damaged skin
  • use only as directed
  • do not apply tight wraps or bandages to treated areas
  • do not apply heat to treated areas immediately before or after use

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • symptoms persist more than 3 days or worsen
  • symptoms clear up and then reoccur within a few days

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply a thin layer to affected areas, massaging onto skin. Repeat as needed. If heat or ice are applied to skin, wait 10 minutes before applying product.

Other information

STORAGE AND HANDLING SECTION

Keep cap firmly in place between uses. Store at room temperature in a dry place. Retain this tip card for full Drug Facts.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Beeswax, Carnauba Oil, Castor Oil, Cocoa Butter, Coconut Oil, Isopropyl Myristate, Lanolin, Mineral Oil, Oleic Acid, Ozoquerite Wax, Stearyl Alcohol.

Questions

OTC - QUESTIONS SECTION

call 210.629.1343

SPL UNCLASSIFIED SECTION

Distributed by
Ona stick
Magnolia, Tx, 77354

PRINCIPAL DISPLAY PANEL - 14 g Tube Blister Pack

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CHAMOMILE • CALENDULA • WITCH HAZEL

Natural active
ingredients

arnica

oná stick®
Pain & bruise balm
Homeopathic medicine

| Wellness at hand.

Goodbye bruises!

Pain & bruise balm
Homeopathic medicine

NET WT 0.5 oz (14 g)

PRINCIPAL DISPLAY PANEL - 14 g Tube Blister Pack
PRINCIPAL DISPLAY PANEL - 14 g Tube Blister Pack

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82610-003-142023-07-28C16284748780-10191ceaa-7150-198a-e063-dbdaa90aec3eARNICA

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82610-003-14ARNICA1 in 1 BLISTER PACKSTICK11
82610-003-14ARNICA14 g in 1 TUBESTICK141

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82610-003ARNICA (ARNICA MONTANA FLOWER, CALENDULA OFFICINALIS FLOWER, HAMAMELIS VIRGINIANA LEAF, AND CHAMOMILE) STICK [ONA STICK USA LLC]1Legacy NDC, 2 package rows20220319_5eea069c-b1ee-44ed-91c1-6cd4979195ff.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82610-00382610-003-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
d36649f0-5f18-4f81-8a19-12ef42b3509a5eea069c-b1ee-44ed-91c1-6cd4979195ff2022-03-17WarningsExact identifier
spl id: d36649f0-5f18-4f81-8a19-12ef42b3509a
spl set id: 5eea069c-b1ee-44ed-91c1-6cd4979195ff

Reported adverse events (FAERS/openFDA)#

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