Carpe Antiperspirant For Feet
Product Images NDC 52261-4700

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Carpe Antiperspirant For Feet (NDC 52261-4700). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cosco International, 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

Insert (4700 Insert)

Text panels contain usage instructions and explanation for Carpe Antiperspirant for Feet. The first panel encourages consistent application twice daily, emphasizing that it takes four weeks of use to see full results. The second panel explains why the product should be applied before bed and the importance of consistent application to build an anti-sweat barrier. Contact information is included.*

FDA Label Image

Tube (4700 1 Tube)

Label for Carpe Antiperspirant for Feet, an antiperspirant foot lotion in a 40 mL (1.35 fl oz) size. The label features the Carpe brand name, directions to apply twice daily, and a Drug Facts panel listing aluminum sesquichlorohydrate as the active ingredient. Distributed by Cosco International, Inc.*

FDA Label Image

Carpe Foot Box 2022

Carpe Antiperspirant for Feet 40 mL (1.35 FL OZ) packaging label features an orange and white design with the Carpe logo. The label includes product information such as use as an antiperspirant foot lotion, dermatologist recommendation, and active ingredient aluminum sesquichlorohydrate (15%). Directions, warnings, inactive ingredients, and contact details for Cosco International, Inc. are also visible.*

* 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.