Strength
120 mg/g
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
51672130005
Classification
Generic
Dosage Form
LOTION
Route
TOPICAL
Last Updated
4/22/2026
Active Ingredients
AMMONIUM LACTATEApproval Type
Generic (ANDA)
FDA Application
ANDA076216On Market Since
5/28/2004
Pharmacological Classes
Acidifying Activity
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