Footspa Pedi Spray
Product Images NDC 49283-702

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Footspa Pedi (NDC 49283-702). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chemco Corporation, 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

Pedi Spray (Antiseptic Pedi Spray 4oz)

FOOTSPA PEDI Antiseptic Pedi Spray with Peppermint & Eucalyptus Oil, 118 mL (4 FL oz) topical spray for use as a foot antiseptic. The label features the brand FootSpa, highlighting a therapeutic effect and use for reducing bacteria on the feet prior to a pedicure. Manufactured by Chemco Corporation, the label includes Drug Facts, directions, warnings, inactive ingredients, and contact information.*

FDA Label Image

Pedi Spray (Antiseptic Pedi Spray 16oz)

FOOTSPA PEDI antiseptic spray with peppermint and eucalyptus oil, topical alcohol-based solution for pedicure use. The label indicates 16 fl oz (473 mL) packaging and highlights its antibacterial protection properties. Manufactured by Chemco Corporation, it includes a drug facts panel listing Ethyl Alcohol 70% as the active ingredient, usage directions, warnings, and contact information.*

FDA Label Image

Pedi Spray (Antiseptic Pedi Spray 128oz)

FootSpa Pedi Spray antiseptic topical spray with peppermint and eucalyptus oil, containing 128 fl oz (3785 mL). The label highlights its use for reducing bacteria and protecting against skin infection. Manufactured by Chemco Corporation, Miami, FL. Includes drug facts panel with active ingredient ethyl alcohol 70% v/v and usage warnings, directions, and ingredient information.*

* 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.