On Duty Unscented
Product Images NDC 10096-5219

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for On Duty Unscented (NDC 10096-5219). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by New Avon Llc, 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

Image Of Dfb (Dfb1)

Drug Facts panel showing the active ingredient Aluminum Chlorohydrate anhydrous at 20.7%, listed as the antiperspirant active ingredient in On Duty Unscented Roll-On Anti-Perspirant Deodorant by New Avon LLC.*

FDA Label Image

Image Of Dfb (Dfb2)

This image shows a text panel with usage information and warnings for On Duty Unscented Roll-On Anti-Perspirant Deodorant. It includes uses like reducing underarm perspiration and lasting 24 hours, warnings for external use only, avoidance of broken skin, stopping use with rash or irritation, advice to ask a doctor if kidney disease is present, and a caution to keep out of reach of children with instructions to seek medical help if swallowed.*

FDA Label Image

Image Of Dfb (Dfb3)

This text panel from On Duty Unscented Roll-On Anti-Perspirant Deodorant provides directions to apply the product to underarms only. It lists inactive ingredients including Water, PPG-15 Stearyl Ether, Steareth-2, Diisopropyl Adipate, and Steareth-20. Contact numbers for questions in the US and Canada are also provided.*

FDA Label Image

Image Of Label (Pdp)

Label of Avon On Duty 24 Hours Unscented Roll-On Anti-Perspirant Deodorant featuring text in blue and white on a gray background. The label indicates the product is unscented, in a 50 ml (1.7 fl. oz.) roll-on lotion form, manufactured by New Avon LLC.*

* 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.