Mometasone Furoate Lotion
Product Images NDC 68462-385

5 FDA label images from Glenmark Pharmaceuticals Inc., Usa · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Mometasone Furoate (NDC 68462-385). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Glenmark Pharmaceuticals Inc., Usa, 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

FDA Label Image

60 mL Carton

60 mL Carton
Mometasone Furoate Topical Solution USP, 0.1% Lotion label for a 60 mL bottle manufactured by Glenmark Pharmaceuticals Inc., USA. The label includes usage warnings such as 'For topical use only' and 'Not for ophthalmic use', with the NDC code 68462-385-02. It also features storage instructions and a caution symbol indicating 'Do not use in eyes.'*
FDA Label Image

Carton 30 mL

Carton 30 mL
The image shows a packaging label for Mometasone Furoate Topical Solution USP, 0.1% lotion, a prescription topical medication by Glenmark Pharmaceuticals Inc. The label includes dosage form (lotion), concentration (0.1%), a 30 mL package size, and warnings such as "For topical use only. Not for ophthalmic use." The NDC number 68462-385-37 is visible along with storage and ingredient details.*
FDA Label Image

Chemical Structure

Chemical Structure
Chemical structure of mometasone furoate, the active ingredient in the topical lotion product Mometasone Furoate 1 mg/mL by Glenmark Pharmaceuticals Inc.*
FDA Label Image

Mometasone Fuoate Usp Structure (Image 01)

Mometasone Fuoate Usp Structure (Image 01)
FDA Label Image
Logo

* 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.