Emj Antiperspirant John Deere Iron Horizon 2.6 Oz Stick
Product Images NDC 60717-651

View Photos of 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 Emj Antiperspirant John Deere Iron Horizon 2.6 Oz (NDC 60717-651). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rna Pharma 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

Active Ingredient (Antiperspirant Flask Ironhorizon 128 064a Back)

Active Ingredient (Antiperspirant Flask Ironhorizon 128 064a   Back)
Drug Facts panel for EMJ Antiperspirant John Deere Iron Horizon 2.6 oz stick, containing 20% Aluminum Zirconium Trichlorohydrex Gly as active ingredient. The label details use for reducing underarm wetness, warnings for external use only, directions to apply underarms only, and a list of inactive ingredients including stearyl alcohol and jojoba seed oil. It also notes 50% recycled plastic packaging, cruelty-free, dermatologist tested, and locally recyclable check.*
FDA Label Image

Purpose Section (Antiperspirant Flask Ironhorizon 128 064a Front)

Purpose Section (Antiperspirant Flask Ironhorizon 128 064a   Front)
Packaging label for EVERY MAN JACK John Deere Iron Horizon Antiperspirant + Deodorant stick, 2.6 oz (73 g). The label highlights 48-hour odor and wetness protection and lists scent notes including sun-warmed amber, cypress, and leather. The active ingredient is Aluminum Zirconium Trichlorohydrex Gly 20%. The label features a wood grain background with the John Deere logo and branding.*

* 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.