Ammonium Lactate Cream
Product Images NDC 51672-1301

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ammonium Lactate (NDC 51672-1301). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Chemical Structure (Ammonium 01)

Chemical structure diagram showing the molecular formula of Ammonium Lactate, a topical cream formulation by Sun Pharmaceutical Industries, Inc. The structure depicts the arrangement of atoms including carboxyl and hydroxyl groups, representing the active ingredient Ammonium Lactate at 120 mg/g strength.*

FDA Label Image

Principal Display Panel (385 g Bottle Label)

Packaging label for Ammonium Lactate Cream 12%, topical cream in a 385 g container. The label lists active ingredients, usage warnings, storage conditions, and manufacturing details, including labeler Sun Pharmaceutical Industries, Inc. The label includes the NDC 51672-1301-0 and states it is Rx only.*

* 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.