Structure (05e2d282 5434 4495 9832 67731f9e7634 01)
Betamethasone Dipropionate Ointment, Augmented
Product Images NDC 68180-947
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Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Betamethasone Dipropionate (NDC 68180-947). 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.
50g-carton (05e2d282 5434 4495 9832 67731f9e7634 02)
This text is a description and prescription details for Betamethasone Dipropionate Ointment USP (Augmented). It includes the NDC number, strength, usage instructions, and dosage information. It also provides information about the manufacturer and storage recommendations. The text is not available.*
Tube Label (05e2d282 5434 4495 9832 67731f9e7634 03)
Betamethasone Dipropionate Ointment USP (Augmented) is a medication used to treat skin conditions such as eczema and psoriasis. The ointment is made of a cement base of propylene glycol and white wax, along with other ingredients. The recommended dosage is to apply a thin layer of the ointment to the affected skin once or twice daily without occlusion. This medication should only be used as directed and is for topical use only. It should be stored at 25°C with excursions permitted between 15° and 30°C. This ointment is manufactured by Lupin Pharmaceuticals and the strength of the medication is expressed as betamethasone. See packaging for lot number and expiration date.*
* 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.
