Outback Pain Relief

Camphor 6%, Menthol 16% · Cream · Topical

Over the counter

Active ingredient

Camphor 6%, Menthol 16%

Purpose

Topical Analgesic

Uses

For the temporary relief of minor aches and pain associated with simple backaches, arthritis, strains, bruises, and sprains.

Warnings

For external use only. When using this product use only as directed, do not bandage tightly or use with a heating pad, avoid contact with eyes or mucous membranes, and do not apply to wounds or damaged skin. Stop use and ask a doctor if condition worsens, if symptoms persist for more than 7 days or clear up and occur again within a few days.

Pregnancy or breast-feeding

If pregnant or breast-feeding ask a health professional.

Keep out of reach of children

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

Directions

Adults and children 12 years of age and older apply generously to the affected area not more than 4 times daily. Children under 12 years of age: ask a doctor.

Inactive ingredients

Benzyl Alcohol, C13-14 Isoparaffin, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Cetearyl Olivate, Cetyl Alcohol, Ethylhexylglycerin, Eucalyptus Globulus Leaf Oil, Glycerin, Laureth-7, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Polyacrylamide, Sorbitan Olivate, Tocopherol, Vanilla Planifolia Fruit Extract, Water.

Label text from the FDA structured product label by Derma Care Research Labs, LLC (revised Dec 20, 2024). Long sections are shortened; the complete label is on DailyMed.

Active ingredients

Camphor (synthetic) in 1 product
Menthol in 1 product

Outback Pain Relief NDC products (1)

NDC	Strength & form	Labeler	Type
72839-987	Camphor (synthetic) 6 g/100g; Menthol 16 g/100g Cream	Derma Care Research Labs, LLC	OTC MONOGRAPH DRUG

Frequently asked questions

What is Outback Pain Relief used for?

For the temporary relief of minor aches and pain associated with simple backaches, arthritis, strains, bruises, and sprains.

Who makes Outback Pain Relief?

Outback Pain Relief is listed by 1 labeler in the FDA NDC directory, including Derma Care Research Labs, LLC.