Lansinoh Anti-itch
Product Images NDC 53997-002

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lansinoh Anti-itch (NDC 53997-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lansinoh Laboratories 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

Display Cartoon (Dc1)

Packaging label for Lansinoh Anti-itch Itch Relief Serum, a topical analgesic by Lansinoh Laboratories Inc. The label highlights moisturizing and relieving dry, itchy skin with organic ingredients and menthol. The 4.4 oz (125 ml) product is dermatologist tested. Drug Facts and warnings for external use are visible, along with directions and inactive ingredients. The label is predominantly purple and green with the Lansinoh logo and website.*

FDA Label Image

Drug Fact And Front (Drug Fact And Front)

Label for Lansinoh Anti-itch Itch Relief Serum, a topical analgesic for temporary relief of itching. The label shows the product volume as 4.4 oz (125 ml) and states it is dermatologist tested. Active ingredient is Menthol 0.5%. The label includes warnings, directions, and a list of inactive ingredients. Distributed by Lansinoh Laboratories Inc, USA.*

FDA Label Image

Front (Front)

Packaging label for Lansinoh Anti-itch Itch Relief Serum by Lansinoh Laboratories Inc, showing a purple and light green tube and outer box. The product is a topical analgesic that relieves itchy skin during pregnancy with soothing organic ingredients. The tube size is 4.4 oz (125 ml), dermatologist tested.*

* 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.