Relieveit Footspray
Product Images NDC 58133-956

2 FDA label images from Cosmetic Specialty Labs, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Relieveit Footspray (NDC 58133-956). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cosmetic Specialty Labs, 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.

Product Images & Figures Index

FDA Label Image

Label (Label Copy File Footspray 00016 1)

Label (Label Copy File Footspray 00016 1)
RelieveIt Footspray Topical Analgesic packaging label by Cosmetic Specialty Labs, Inc. The label features a blue and pink background with a silhouette of a woman holding a dandelion. It highlights the product as a footspray with fast-acting and long-lasting effects, pleasant scent, and stain-free properties. The package includes one 0.5 oz twist-up canister with a refill. The label also displays drug facts and usage information on the right side, as well as the product website and a barcode at the bottom.*
FDA Label Image

Refill (Label Copy File Refill 00010 1)

Refill (Label Copy File Refill 00010 1)
RelieveIt Footspray topical analgesic packaging label features a silhouette of a woman with a dandelion against a sky background with clouds. The label highlights the product as a refill spray with menthol as active ingredient (8%). It mentions benefits like fast-acting, long-lasting relief, pleasant scent, and stain-free formula. Manufactured by Cosmetic Specialty Labs, Inc., the label includes drug facts, warnings, directions, and storage instructions.*

* 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.