Active Ingredient: AMMONIUM LACTATE
Proprietary Name: LAC-HYDRIN
Dosage Form; Route of Administration: LOTION; TOPICAL
Strength: EQ 12% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019155
Product Number: 001
Approval Date: Apr 24, 1985
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information