Drugplain

ARTREX 3 g/60g

Camphor, Menthol, and Turpentine · CREAM · Bioved Pharmaceuticals

No Recall History
Plain English

ARTREX is a cream containing camphor, menthol, and turpentine at 3 g/60g, taken topical. Manufactured by Bioved Pharmaceuticals.

Key Facts

Brand Name
ARTREX
Generic Name
Camphor, Menthol, and Turpentine
NDC Code (Product)
68354-131
Manufacturer
Bioved Pharmaceuticals
Strength
3 g/60g
Dosage Form
CREAM
Route
TOPICAL
Marketing Status
Application #
M014
Marketing Start
04/01/2004

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Temporarily relieves aches and pains of muscles and joints due to arthritis, simple backache, sprains, strains, and sports injuries

Dosage & Administration

Adults and children 6 years of age and older Apply to affected area 3-4 times a day

Warnings

Do not apply to wound or damaged skin Do not bandage tightly Do not swallow. If swallowed call a physician or contact a poison control center immediately Keep away from eyes, mucous membranes, broken or irritated skin If skin redness or irritation develops or pain lasts more than 10 days, discontinue use and call a physician

Frequently Asked Questions

What is ARTREX used for?

ARTREX contains Camphor, Menthol, and Turpentine. It is a cream taken topical. Consult your doctor for specific uses.

Is ARTREX a controlled substance?

ARTREX is not classified as a controlled substance by the DEA.

What is the generic name for ARTREX?

The generic name for ARTREX is Camphor, Menthol, and Turpentine. There are no other listed brand versions of Camphor, Menthol, and Turpentine.

What is the NDC code for ARTREX 3 g/60g?

The NDC (National Drug Code) for ARTREX 3 g/60g is 68354-131, listed by Bioved Pharmaceuticals.

Product NDC

68354-131

Package NDC

68354-131-10

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)