Real Time Pain Relief Foot Cream
Product Images NDC 84573-515

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Real Time Pain Relief Foot (NDC 84573-515). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Real Time Products 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

Label01.jpg (Label01)

Label01.jpg (Label01)
Real Time Pain Relief Foot Cream contains menthol 15 mg/g as the active ingredient in a topical analgesic cream form. The 4.4 oz (125 g) packaging highlights temporary relief from arthritis, muscle strains, sprains, bruises, and cramps. The label also lists Real Time Products Inc. as the distributor and includes directions for use and drug facts.*
FDA Label Image

Label02.jpg (Label02)

Label02.jpg (Label02)
Real Time Pain Relief Foot Cream 15 mg/g Menthol topical analgesic cream in a 6 oz (170 g) size. The label highlights temporary relief from arthritis, muscle strains, sprains, bruises, and cramps. Labeler is Real Time Products Inc., with product barcode and detailed drug facts including active/inactive ingredients, warnings, and directions for use.*
FDA Label Image

Label03.jpg (Label03)

Label03.jpg (Label03)
Real Time Pain Relief Foot Cream is a topical analgesic cream containing menthol 15 mg/g, provided by Real Time Products Inc. The label states it offers temporary relief from arthritis, muscle strains, sprains, bruises, and cramps. The package size is 8 oz (226 g) and includes Drug Facts, directions for use, and a barcode.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.