Banish My Pain

Manufacturer
LAIDEN MONTANA EMU PRODUCTS
Effective date
2019-05-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:59:26

Label at a glance#

ProductBanish My Pain
Active ingredientCAMPHOR (NATURAL)
Label structure8 sections

Indications and uses

for the temporary relief of minor aches and pains of muscles and joints associated with: simple backache arthritis strains bruises sprains

Dosage and administration

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. massage into area until thoroughly absorbed Children under 2 years of age: consult a doctor.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Camphor 4.6%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

for the temporary relief of minor aches and pains of muscles and joints associated with:

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • on wounds or damaged skin
  • with a heating pad

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes and mucous membranes
  • do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

INSTRUCTIONS FOR USE SECTION

  • Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
  • massage into area until thoroughly absorbed
  • Children under 2 years of age: consult a doctor.

Other information

OTHER SAFETY INFORMATION

  • Best stored at room temperature or cooler.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Helianthus Annuus (Sunflower) Seed Oil, Emu Oil, Beeswax, Butyrospermum Parkii (Shea) Butter, Arnica Montana Flower, Calendula Officinalis (Calendula) Flower, Melissa Officinalis (Lemon Balm) Leaf, Chamomilla Recutita (Chamomile) Flower, Tocopherol, Melaleuca Leucadendron Cajaputi (Cajeput) Oil, Lavandula Angustifolia (Lavender) Oil, Eucalyptus Globulus (Eucalyptus) Leaf Oil, Chamomilla Recutita (Chamomile) Oil, Citrus Grandis (Grapefruit) Seed Extract.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72895-081-022021-01-29C16284748780-1ba0f9c33-4545-a910-e053-dadaa90a0b85Banish My Pain

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72895-081-02Banish My Pain60 mL in 1 JAROINTMENT601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72895-081BANISH MY PAIN (CAMPHOR) OINTMENT [LAIDEN MONTANA EMU PRODUCTS]1Legacy NDC, 1 package rows20190509_883d65e1-78aa-be9d-e053-2a95a90aa591.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
72895-08172895-081-02

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
883d65e1-78a9-be9d-e053-2a95a90aa591883d65e1-78aa-be9d-e053-2a95a90aa5912019-05-06WarningsExact identifier
spl id: 883d65e1-78a9-be9d-e053-2a95a90aa591
spl set id: 883d65e1-78aa-be9d-e053-2a95a90aa591

Reported adverse events (FAERS/openFDA)#

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