Collagenase Santyl Ointment
Product Images NDC 50484-010

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Collagenase Santyl (NDC 50484-010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Smith & Nephew, 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

2228603f-figure-01 (2228603f Figure 01)

SANTYL Ointment is a product of Smith & Nephew, used for enzymatic debridement to remove dead tissue. It contains 250 units of Collagenase derived from Clostridium histolyticum per gram and does not contain preservatives. It is for external use only and should not be stored over 25°C (77°F). The tube should be punctured from the cap's inverted end, which keeps it sterile until opened. The prescribing information is enclosed. The U.S standard of potency is not available. The product is only sold with a prescription.*

FDA Label Image

2228603f-figure-02 (2228603f Figure 02)

SANTYL Ointment with Collagenase, containing 250 units per gram, is an enzymatic drug prescribed for external use only. The tube must not be stored above 25°C (77°F) and must not be used beyond the expiry date. The drug does not contain any preservatives, and sterility is assured until the tube is opened by puncturing the cap. This government-licensed drug is manufactured by Smith & Nephew in Fort Worth, TX, and is marketed by Smith & Nephew across the United States. For more information, see the attached prescribing instructions or contact 1-800-441-8227.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.