Menthol
Product Images NDC 50488-1040

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Menthol (NDC 50488-1040). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alexso, Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Principal Display Panelndc 50488-1040-1menthol 4% Cream120 Grams (Menthol Cream 01)

Principal Display Panelndc 50488-1040-1menthol 4% Cream120 Grams (Menthol Cream 01)
This is a description of a topical analgesic drug containing menthol, indicated for the temporary relief of minor aches and pains of muscles and joints. The drug can be applied externally up to 3 to 4 times a day, and it should not be used on children under 2 years without advice from a doctor. It is not suitable for wounds or damaged skin. Inactive ingredients include arnica, boswellia extracts, and various glycerins and alcohols. The drug should not be used in large quantities, particularly over raw surfaces or blistered areas, and caution should be taken to avoid contact with the eyes. Adverse reactions include redness, swelling, pain or other symptoms, and use should be discontinued if they occur, or if the condition worsens or doesn't improve within 7 days. This drug should be kept out of the reach of children.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.