Ammonia
Product Images NDC 68599-7100

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ammonia (NDC 68599-7100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mckesson, 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

Drug Fact (10104 Box Drug Facts)

Packaging label for McKesson Ammonia inhalants, labeled as 15% to 35% strength. The label includes drug facts with active ingredient Ammonia 15% as an inhalant. It provides warnings, directions, and inactive ingredients such as alcohol USP and several oils. The label shows a package quantity of 100 inhalants, net contents of 0.01 fl oz each, and includes a barcode, manufacturer number 10104, and distributor information for McKesson Medical-Surgical Inc.*

FDA Label Image

Case (10104 Case)

Label for Ammonia Inhalants by McKesson, showing strength range of 15% to 35%. The label states net contents of 0.01 fl oz (0.3 mL) with 100 units per box and 108 boxes per case. Manufacturer number is 10104. Distributed by McKesson Medical-Surgical Inc., Richmond, VA, made in the USA. Includes a barcode and a customer service phone number.*

FDA Label Image

Box (10104 Box)

Packaging label for McKesson Ammonia Inhalants indicating a concentration range of 15% to 35% strength. The label states a net content of 0.01 fluid ounces (0.3 mL) per unit, with 100 units per box. Includes instructions that the product is used to prevent or treat fainting and a warning not to reuse the inhalants. The manufacturer number is 10104.*

* 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.