Calcipotriene Solution
Product Images NDC 0713-0318

3 FDA label images from Cosette Pharmaceuticals, 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 Calcipotriene (NDC 0713-0318). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cosette 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

Label (Label)

Label (Label)
Carton label for Calcipotriene Topical Solution 0.005% (Scalp Solution) by Cosette Pharmaceuticals, Inc. The 60 mL prescription drug is indicated for topical dermatologic use only and is flammable, containing 0.05 mg/mL calcipotriene in a solution with isopropyl alcohol and other ingredients. The label includes usage warnings, dosage instructions, storage conditions, NDC 0713-0318-53, and a barcode.*
FDA Label Image

Formula (Structure)

Formula (Structure)
Chemical structure diagram of the active ingredient Calcipotriene, illustrating its molecular composition with bonds and functional groups indicated in a skeletal formula.*
FDA Label Image

Tube (Tube)

Tube (Tube)
The image shows the label for Calcipotriene Topical Solution 0.005% (Scalp Solution) in a 60 mL bottle, manufactured by Cosette Pharmaceuticals, Inc. The label includes dosage form as topical solution with a concentration of 0.05 mg/mL. It notes the product is for topical dermatologic use only, not for ophthalmic, oral, or intravaginal use, and lists storage instructions and warnings including flammability. The NDC 0713-0318-53 is displayed along with barcode and distributor information.*

* 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.