Calasoothe Ointment
Product Images NDC 67777-241

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Calasoothe (NDC 67777-241). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dynarex Corporation, 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

1271_bx_master (1271 Bx Master R260629 1)

CalaSoothe Skin Protectant anorectal (hemorrhoidal) ointment containing calamine USP 5%, menthol USP 0.44%, and zinc oxide USP 20.625%. The ointment is presented in a 3.5 g net weight package with 144 packets. Labeler is Dynarex Corporation. The packaging highlights product purposes such as drying oozing poison, relieving itching and discomfort, and providing a cooling sensation.*

FDA Label Image

1273_in_master (1273 In Master R260629 1)

CalaSoothe ointment label for a skin protectant containing Calamine USP 5%, Menthol USP 0.44%, and Zinc Oxide USP 20.625%. It is indicated as an anorectal (hemorrhoidal) ointment with a net weight of 2.5 oz (71 g). The label features product benefits such as calming, cooling, and skin protection, and it is manufactured by Dynarex Corporation.*

FDA Label Image

1275_in_master (1275 In Master R260629 1)

The CalaSoothe ointment packaging label features the active ingredients Calamine USP 5%, Menthol USP 0.44%, and Zinc Oxide USP 20.625%. It is labeled as an anorectal (hemorrhoidal) ointment with skin protectant properties. The net weight is 4 oz (113 g), with Dynarex Corporation as the manufacturer. The label includes drug facts, usage warnings, directions, and inactive ingredients, along with a barcode and contact 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.