Betamethasone Valerate
Product Images NDC 67296-2080

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Betamethasone Valerate (NDC 67296-2080). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Graphical User Interface, Text, Application

description Automatically Generated (Betame 1)

Label for Betamethasone Valerate Cream, USP 0.1% strength, 15 g tube. Contains usage instructions, warnings, and storage information. Distributed by Cosette Pharmaceuticals, Inc. The label includes the NDC 0713-0326-15 and emphasizes the product is for dermatologic use only, not for ophthalmic use.*

FDA Label Image

Text

description Automatically Generated (Betame 2)

Betamethasone Valerate Cream, USP 0.1%, 15 g tube carton by RedPharm Drug. The packaging displays the active ingredient strength, usage instructions, and a warning that it is for dermatologic use only and not for ophthalmic use. The label also includes manufacturer details, a barcode, and tamper-evident seal instructions.*

FDA Label Image

Graphical User Interface, Text, Application

description Automatically Generated (Betame 3)

Label for Betamethasone Valerate Cream, USP 0.1%, 45 g tube for dermatologic use only. The label shows potency as betamethasone, cautions against ophthalmic use, and includes usage instructions, storage conditions, warnings, and distributor information from Cosette Pharmaceuticals, Inc. The label also features barcodes and a seal opening instruction.*

FDA Label Image

Text

description Automatically Generated (Betame 4)

Packaging label for Betamethasone Valerate Cream, USP 0.1%, 45g tube. The label includes directions for use, caution for dermatologic use only, and tamper-resistant seal instructions. The label is from Cosette Pharmaceuticals, Inc. and features the NDC 0713-0326-37 barcode with a mustard yellow and black color scheme.*

FDA Label Image

Text

description Automatically Generated (Betame 5)

Betamethasone Valerate 0.1% ointment label showing 15 g package size. The label indicates the product is for dermatologic use only, with dosage instructions and storage information. The label also includes warnings, manufacturer details (Cosette Pharmaceuticals Inc.), and NDC barcode.*

FDA Label Image

Graphical User Interface, Text

description Automatically Generated (Betame 6)

Betamethasone Valerate Ointment, USP 0.1% strength, 15 g tube packaging label. The label states it is for dermatologic use only and not for ophthalmic use. Distributed by Cosette Pharmaceuticals, Inc. The package includes usage instructions and warnings. The label shows Rx only and a barcode.*

FDA Label Image

Text

description Automatically Generated (Betame 7)

Label for Betamethasone Valerate 0.1% ointment, USP, in a 45 gram package. The label includes usage warnings, storage instructions, and directions for opening. Distributed by Cosette Pharmaceuticals, Inc., with a barcode and NDC code 0713-0327-37.*

FDA Label Image

Text

description Automatically Generated (Betame 8)

The unfolded carton packaging for Betamethasone Valerate Ointment, USP 0.1%, 45 g. The box displays the product name, strength, and dosage form prominently on a white and gold background. It indicates the product is for dermatologic use only and not ophthalmic use. Additional text includes dosage instructions and storage information. The labeler RedPharm Drug is mentioned along with various codes including NDC and GTIN barcodes.*

FDA Label Image

Structural Formula (Structure)

Chemical structure diagram of betamethasone valerate showing its molecular formula (C27H37FO6) and molecular weight (476.59). The structure depicts the steroid backbone with various functional groups attached, including hydroxyl, carbonyl, and fluorine substituents.*

* 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.