Mometasone Furoate Solution
Product Images NDC 72162-1392
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Product Visual Gallery
This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Mometasone Furoate (NDC 72162-1392). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Bryant Ranch Prepack, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
Label (Lbl721621392)
This text appears to be a description of a medication called "Mometasone Furoate Topical Solution, USP". Each gram of this solution contains 1 mg of Mometasone Furoate. The solution is made up of various ingredients, including isopropyl alcohol, hexylene glycol, hydroxypropyl cellulose, sodium phosphate monobasic anhydrous, purified water, glycerin, and oleic acid. The pH of the solution is adjusted to approximately 4.5 using phosphoric acid. It is specified that this medication should be kept out of reach of children and stored at a temperature between 20°C and 25°C (68°F to 77°F). The medication is for dermatologic use only and should not be used for ophthalmic purposes. The NDC (National Drug Code) for this medication is 72162-1392-3. The medication is packaged in a 30 mL (275 g) container and has been relabeled by Bryant Ranch Prepack, Inc. It was originally manufactured by Padagis in Burbank, CA, USA. Unfortunately, the last line contains non-English characters and is not readable.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.