CLINICAL STUDIES

Years of extensive research and clinical studies were done to prove the efficacy of Lactezin in the following:

  • Reduction of total lesions (whiteheads, blackheads and pimples)
  • Reduction of oiliness
  • Reduction of pore size

Studies were conducted among males and females aged 13 to 40 and above suffering from mild to moderate acne.

AND THE RESULTS ARE CLEAR

  • The study showed a significant reduction of total lesions as early as 2 weeks
  • After 2 weeks of use, there was also significant reduction of oiliness of the face, and significant improvements in the skin.

No serious adverse event leading to the discontinuation of the product were noted during the study. Moreover, none of the subjects experienced product related adverse events over the duration of the study.

If symptoms persist, consult your doctor.
Reference: Data on file (Innovitelle Clinical Study)

OTHER DOWNLOADABLE STUDIES


A Randomized, Double-Blind, Placebo-Controlled Trial to Determine the Efficacy and Safety of Lactoferrin with Vitamin E and Zinc as an Oral Therapy for Mild to Moderate Acne Vulgaris

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ASC Ref. No. U006P040517L, I073N080618L, I088N080618L, I094N080618L, I113N080618L, I010N081318L, I013N081318L, I014N081318L, I020N081318L, I022N081318L

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