Chemical Structure (Ammonium 01)
Ammonium Lactate Cream
Product Images NDC 51672-1301
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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.
Product Images & Figures Index
Principal Display Panel (385 g Bottle Label)
This is a description of a medication containing ammonium lactate for dermatological use only. It contains 12% ammonium lactate (as equivalent to lactic acid), cetyl acobol, glycerin, glyceryl monostearate, Taureth-,ight mineral i, magnesium aluminum silate, methylcellulose, methyiparaben, propylparaben, polyoxyethyiens - 100 tearate, poyoxyi 40 stearate, propylene glycol, purified water for pH adjustment. Apply it twice daily or as directed by a physician. This medication is manufactured and distributed by Taro Pharmaceuticals, and it is not for ophthalmic, oral, or intravaginal use. The package insert should be consulted for full prescribing information. Store it between 20°-25° (68°-77°F). It is RX only.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
