Centurion Labz

Retreat

Serving
3 Capsule(s)
Per container
60
Form
capsule-unknown
DSLD
Formula hash
7efa744ef973
Brand context
Catalog
15
products
With avoid flag
0
products
FDA recalls
0
history
CAERS
1
reports
Caution-flaggedObjective label signals
Flagged excipients
5
0 avoid · 5 caution
FDA recalls
0
no recall history
CAERS reports
1
FDA consumer events
Certifications
0
none recorded
5 excipients carry authority-caution citations. · Every flag below links to the authority's published citation.
NIH LiverTox
1 ingredient with hepatotoxicity classification
Worst severity: Category D
About LiverTox →
  • Saw PalmettoCategory D

    LiverTox Category D. Rare cases of acute hepatitis reported; causality uncertain. Some reports confounded by concurrent pharmaceuticals.

    LiverTox →

Supplement Facts

5 active ingredients
IngredientAmount% DV
D-Aspartic Acid, Powder
D-Aspartic Acidamino_acidUNII · 4SR0Q8YD1X
1500 mg
Fenugreek
herbUNII · 654825W09Z
350 mg
Saw Palmetto
herbUNII · J7WWH9M8QS
LiverTox D
160 mg
Androst-3, 5-dien-7, 17-dione
Arimistaneherb
75 mg
Diindolylmethane
herbUNII · SSZ9HQT61Z
50 mg
Flagged excipients

5 flagged · authority citations

  • ◐ CAUTIONFD&C Blue #1
    color

    EU requires 'attention in children' warning per Commission Regulation 1333/2008 Annex III. Limited to specific food categories; capsule-shell use permitted with restrictions.

  • ◐ CAUTIONFD&C Green #3
    color

    Banned in EU countries (not listed in Reg 1333/2008 Annex II). Permitted in US under 21 CFR 74.203. Used in some capsule coatings.

  • ◐ CAUTIONFD&C Red #3
    color

    FDA revoked food/ingested-drug color additive approval for FD&C Red 3 in January 2025 (Docket FDA-2022-C-2886). Manufacturers have until January 2027 (foods) / January 2028 (ingested drugs) to reformulate.

  • ◐ CAUTIONFD&C Red #40
    color

    EU requires the same 'attention/activity in children' warning label as Yellow 5 per Commission Regulation 1333/2008 Annex III. California enacted a public-school ban effective 2028 (AB 2316, 2024).

  • ◐ CAUTIONFD&C Yellow #6
    color

    EU requires 'attention in children' warning per Reg 1333/2008 Annex III (Southampton study 2007). Banned in Norway + Finland; allowed in US under 21 CFR 74.706 with declaration.

FDA CAERS · adverse event context
1
consumer-submitted adverse event reports filed with the FDA CFSAN Adverse Event Reporting System mentioning this product or its brand.

CAERS reports are unverified consumer submissions — not adjudicated causality. Large well-known brands accumulate proportionally more reports simply due to broader use. About CAERS →

Other ingredients

Gelatin · Magnesium Stearate · Silicon Dioxide