Gold Bond Medicated Extra Strength Body Powder
Product Images NDC 84714-0410

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 Gold Bond Medicated Extra Strength Body (NDC 84714-0410). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gold Bond Co 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

Goldbondextra Strengthbody Powdernet Wt 10 Oz (283 G) (Gold Bond Medicated Extra Strength Body Powder 01)

Goldbondextra Strengthbody Powdernet Wt 10 Oz (283 G) (Gold Bond Medicated Extra Strength Body Powder 01)
Label of Gold Bond Medicated Extra Strength Body Powder containing Menthol 0.8%, a topical powder for anti-itch relief. The package highlights a triple action formula that absorbs, cools, and controls odor, is talc-free, and has a net weight of 10 oz (283 g). Manufactured by Gold Bond Co LLC.*
FDA Label Image

Principal Display Panelgoldbondextra Strengthbody Powdernet Wt 10 Oz (283 G) (Gold Bond Medicated Extra Strength Body Powder 02)

Principal Display Panelgoldbondextra Strengthbody Powdernet Wt 10 Oz (283 G) (Gold Bond Medicated Extra Strength Body Powder 02)
Drug Facts panel from Gold Bond Medicated Extra Strength Body Powder. It lists menthol 0.8% as the active anti-itch ingredient, use for minor cuts, sunburn, insect bites, scrapes, minor burns, and skin irritations, warnings for external use only, directions for use by age, and inactive ingredients including corn starch and zinc oxide. The label also includes manufacturer details, barcode, and recycling 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.