Kiwi Antiperspirant Deodorant Roll-on Cream
Product Images NDC 84178-009

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Kiwi Antiperspirant Deodorant Roll-on (NDC 84178-009). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Evi Labs, 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

Kiwi Back Render (Kiwi Back Render)

Back label of KIWI ANTIPERSPIRANT DEODORANT ROLL-ON cream with green cap and white container. The label includes Drug Facts detailing active ingredient aluminum chlorohydrate 10% as antiperspirant, uses, warnings, directions, and a list of inactive ingredients including fragrance, kiwi extract, and others. Distributor is Zermat USA Inc., Houston, TX. Barcode included.*

FDA Label Image

Kiwi From Render (Kiwi From Render)

KIWI ANTIPERSPIRANT DEODORANT ROLL-ON cream in a white bottle with a green cap. The front label shows the brand name Zermat and product name "Kiwi". Additional text indicates long-lasting fragrance with kiwi extract. Net weight is 2.82 oz.*

FDA Label Image

Kiwi Panel (Kiwi Panel)

Drug Facts label from KIWI ANTIPERSPIRANT DEODORANT ROLL-ON cream showing active ingredient Aluminum chlorohydrate 10% as an antiperspirant. The label includes use instructions, warnings for external use, directions to apply to underarms only, and a list of inactive ingredients including fragrance and kiwi extract. Also displays distributor contact information 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.