Original Pain Relief Cream

Manufacturer
Ultra Mix (Aust) Pty Ltd
Effective date
2015-02-16
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:20:15

Label at a glance#

ProductOriginal Pain Relief Cream
Active ingredientEUCALYPTUS OIL, TEA TREE OIL
Label structure6 sections

Dosage and administration

Apply a small amount of  Original Pain Relief Cream to the affected area & gently massage in until fully absorbed. Use twice daily or more frequently if required.

Label contents#

Full prescribing information#

Actives

OTC - ACTIVE INGREDIENT SECTION

Tea Tree Oil (Melaleuca Alternifolia) - 42.5 mg/g
Eucalyptus Oil (Eucalyptus radiata) - 38.6 mg/g

Purpose

OTC - PURPOSE SECTION

Pain relief cream to assist with relief of joint and muscle pain.

Indication and Usage

INDICATIONS & USAGE SECTION

For the temporary relief of arthritic pain & relief of muscular aches & pains, including symptomatic relief of lower back pains. May

also assist with increased joint mobility & reduce inflammation and swelling associated with arthritis and gout.

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Apply a small amount of  Original Pain Relief Cream to the affected area & gently massage in until fully absorbed. Use

twice daily or more frequently if required.

Warnings

WARNINGS SECTION

For external use only.

Ensure safety seal is intact beforeopening. Keep tube sealed when not being used. Store below 300 C (86 F).

If symptoms persist seek the advice of a health care practioner.

Keep out of reach from children.

Product Carton Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

pain-reliefpain-relief

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69594-004-012020-01-31C16284748780-19d75b9d1-099c-f424-e053-dadaa90a57ceOriginal Pain Relief Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69594-004-01Original Pain Relief Cream100 g in 1 TUBECREAM1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69594-004ORIGINAL PAIN RELIEF CREAM (EUCALYPTUS OIL AND TEA TREE OIL) CREAM [ULTRA MIX (AUST) PTY LTD ]1Legacy NDC, 1 package rows20150217_98572928-c809-48f6-9597-6105e2e6ed61.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
EUCALYPTUS OILACTIVE INGREDIENT2R04ONI6621
TEA TREE OILACTIVE INGREDIENTVIF565UC2G1
EUCALYPTUS OILACTIVE MOIETY2R04ONI6621
TEA TREE OILACTIVE MOIETYVIF565UC2G1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69594-00469594-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
EUCALYPTUS OIL2R04ONI662ACTIB
TEA TREE OILVIF565UC2GACTIB

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
412d447f-56dc-4f62-8e5d-e4ce38bd0de898572928-c809-48f6-9597-6105e2e6ed612015-02-16WarningsExact identifier
spl id: 412d447f-56dc-4f62-8e5d-e4ce38bd0de8
spl set id: 98572928-c809-48f6-9597-6105e2e6ed61

Reported adverse events (FAERS/openFDA)#

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