Betamethasone Dipropionate Cream
Product Images NDC 70710-1233

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

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Betamethasone Dipropionate (NDC 70710-1233). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Pharmaceuticals Usa 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.

Product Images & Figures Index

FDA Label Image

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24da9737 A6ca 4aeb B7ad 5c44b9365b52 01
Chemical structure of the active ingredient betamethasone dipropionate, showing its steroid backbone with functional groups including hydroxyl, fluorine, ketone, and two propionate ester groups.*
FDA Label Image

24da9737 A6ca 4aeb B7ad 5c44b9365b52 02

24da9737 A6ca 4aeb B7ad 5c44b9365b52 02
Label for Betamethasone Dipropionate Cream USP 0.05% topical cream by Zydus Pharmaceuticals USA Inc. The label indicates a quantity of 15 grams and notes the product is for dermatologic use only, not for ophthalmic use. It includes dosage information, storage instructions, and manufacturer details for Cadila Healthcare Ltd., India, with distribution in the USA by Zydus Pharmaceuticals (USA) Inc.*
FDA Label Image

24da9737 A6ca 4aeb B7ad 5c44b9365b52 03

24da9737 A6ca 4aeb B7ad 5c44b9365b52 03
Packaging label for Betamethasone Dipropionate Cream USP 0.05%, a topical human prescription drug. The carton displays the active ingredient strength as 0.05% (potency expressed as betamethasone), with a quantity of 15 grams per container. The labeler is Zydus Pharmaceuticals USA Inc. The label includes usage warnings and storage instructions, and features the NDC number 70710-1233.*

* 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.