Original Pain Relief Cream
FDA Label NDC 69594-004

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ultra Mix (aust) Pty Ltd for the product Original Pain Relief Cream (NDC 69594-004). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding actives, purpose, indication and usage, dosage and administration, warnings, product carton label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Actives

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

Purpose

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

Indication And Usage

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

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

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

Pain-relief (Pain Relief)

Pain-relief (Pain Relief)

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