Clobetasol Propionate Ointment
Product Images NDC 43386-096

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Clobetasol Propionate (NDC 43386-096). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals,inc., 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

Structure (370129be 84f5 4edf B821 Ffbad2db8c66 01)

Chemical structure diagram of clobetasol propionate, showing its molecular framework with various functional groups including ketones, chloromethyl, and fluorine substituents characteristic of this topical corticosteroid.*

FDA Label Image

15 G (Container)

Clobetasol Propionate Ointment USP 0.05% topical ointment label with NDC 43386-096-60, manufactured by Lupin Pharmaceuticals, Inc. The label includes usage warnings, storage instructions, and directions for puncture-cap opening. The package size is 15 grams. It is for dermatologic use only and not for ophthalmic use.*

FDA Label Image

60 G (Carton)

Clobetasol Propionate Ointment USP 0.05% topical ointment packaging label. The 15 g carton displays the product name, strength, route of administration, and manufacturer Lupin Pharmaceuticals, Inc. Directions for use notes dermatologic use only and Rx only status. Batch coding and storage instructions are also visible on the label.*

FDA Label Image

30g Conatiner (370129be 84f5 4edf B821 Ffbad2db8c66 04)

Label for Clobetasol Propionate Ointment USP 0.05% topical ointment, 30 g, manufactured by Lupin Pharmaceuticals, Inc. The label includes usage warnings, storage instructions, a barcode, and manufacturing details indicating production in India and the United States.*

FDA Label Image

30g Carton (370129be 84f5 4edf B821 Ffbad2db8c66 05)

Clobetasol Propionate Ointment USP 0.05% topical ointment carton by Lupin Pharmaceuticals, Inc. The 30 g package is prescription-only and labeled for dermatologic use, not for ophthalmic use. It includes batch code and storage instructions and indicates it is manufactured by Lupin Limited in India for Lupin Pharmaceuticals in the U.S.*

FDA Label Image

45g Container (370129be 84f5 4edf B821 Ffbad2db8c66 06)

Clobetasol Propionate Ointment USP 0.05% topical ointment label by Lupin Pharmaceuticals, Inc. The label shows the active ingredient concentration as 0.05%, net weight 45 grams, and contains storage and usage warnings. Manufactured by Lupin Limited, India, with a prominent NDC 43386-096-63 and barcodes on the right side.*

FDA Label Image

45g Carton (370129be 84f5 4edf B821 Ffbad2db8c66 07)

Packaging label for Clobetasol Propionate Ointment USP 0.05% topical ointment, 45 g tube, manufactured and labeled by Lupin Pharmaceuticals, Inc. The label indicates this product is for dermatologic use only and is prescription-only. The label includes usage instructions, storage directions, barcode, and manufacturing information for Lupin Limited, India.*

FDA Label Image

60g Container (370129be 84f5 4edf B821 Ffbad2db8c66 08)

Label for Clobetasol Propionate Ointment USP 0.05% topical ointment, 60 g tube, by Lupin Pharmaceuticals, Inc. The label highlights that it is for dermatologic use only and not for ophthalmic use. Packaging details include storage instructions, manufacturer info, and a barcode.*

FDA Label Image

60g Carton (370129be 84f5 4edf B821 Ffbad2db8c66 09)

Packaging label for Clobetasol Propionate Ointment USP 0.05% topical ointment, 60 grams, by Lupin Pharmaceuticals, Inc. The label includes product and strength details, usage cautions for dermatologic use only, manufacturing information, and storage instructions. The NDC number 43386-096-62 is displayed along with barcodes.*

* 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.