HOW WAS THE KLARSKIN RADIANCE POWDER TESTED IN CLINICAL TRIALS? AND DOES IT ACTUALLY WORK? 

Before pictures were taken of clinical trial participants and a skin analysis was performed on each patient on day 1 and day 30 of the trial.

The Sebumeter SM815 Machine System was used for impartial skin condition testing on each trial participant.

Clinical Trial participants consumed 5grams, the equivalent of 1 Spoon of the Radiance Powder mixed with 200ml of filtered water, 15 minutes before any food consumption each morning. All trial participants consumed the total 30-day dose continuously, without a break in days.

 "90% of trial participants saw an improvement in Acne Vulgaris after 30 days of use"

"80% of trial participants had improvement in the overall appearance of their skin"

"80% of trial participants had reduced redness and inflammation on their skin" 

Read the full clinical trial below, and keep scrolling for our before & after customer experiences with the Radiance Powder 

SCIENTIFIC RESULTS OBTAINED AFTER 30 DAYS 

An independent dermatologist study was also done on the Radiance Powder and we were awarded the following certificates: 

1. Certificate of Excellence for sensitive skin under Dermatological Review

2. Certificate of Excellence for irritant prone skin under Dermatological Review

• 90% of trial participants saw an improvement in Acne Vulgaris after 30 days of use

• 80% of trial participants had improvement in the overall appearance of their skin

• 80% of trial participants had reduced redness and inflammation on their skin

• 80% of trial participants had improved gut and digestive health

• 70% of trial participants stated the Radiance Powder was better, or much better, compared to other products previously used to help clear acne vulgaris

Neither intolerance reactions suggestive of irritation nor allergic reactions (contact dermatitis) were detected in clinical trial subjects during the entire process.

THE FOLLOWING RESULTS WERE MEASURED USING THE SEBUMETER SM815 MACHINE SYSTEM. THE RADIANCE POWDER ACHIEVED:

• A REDUCTION IN PORPHYRINS OF 17.22%

• A REDUCTION IN REDNESS OF 14.37%

• A REDUCTION IN PORES OF 20.47%

• A REDUCTION IN COMEDONES OF 28.07%

• A REDUCTION IN PAPULES OF 33.69%

• A REDUCTION IN PUSTULES OF 41.91%

The following are before and after pictures from the test subjects who took part in the clinical trial where permission and rights were obtained for the use of the photo imagery: