Menthol And Zinc Oxide Ointment
Product Images NDC 67777-234

View Photos of 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 Menthol And Zinc Oxide (NDC 67777-234). 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 (r220513 1)

1271 Bx Master (r220513 1)
Packaging label for We Care CalaSoothe ointment from Dynarex Corporation, containing Menthol 0.44% and Zinc Oxide 20.625%. The label indicates it is a topical ointment available in 144 packets, each with a net weight of 3.5 g. The product protects, soothes, and promotes healing, with directions and drug facts included on the label.*
FDA Label Image

1271 Bx Stis010 (r220513 1)

1271 Bx Stis010 (r220513 1)
Packaging label for CALASOOTHE ointment containing Menthol 0.44% and Zinc Oxide 20.625%. The label states it is a topical ointment that protects, soothes, and promotes healing. It is manufactured for Dynarex Corporation and distributed under the We Care brand. The package contains 144 packets, each with a net weight of 3.5 g.*
FDA Label Image

1275 In Master (r220513 1)

1275 In Master (r220513 1)
Drug Facts label for Calasoothe ointment by Dynarex Corporation. It lists active ingredients menthol 0.44% as external analgesic and zinc oxide 20.625% as skin protectant. Includes uses for skin irritation relief, warnings for external use, directions for application, storage info, inactive ingredients, and contact details.*

* 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.