supplementhackr
Truvy

Tru

Serving
1 Capsule(s)
Per container
15
Form
capsule-unknown
DSLD
264530
Formula hash
c2140289addf
Brand context
Truvy
Catalog
4
products
With avoid flag
2
products
FDA recalls
0
history
CAERS
30
reports
Avoid-flaggedObjective label signals
Flagged excipients
3
1 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
30
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

7 active ingredients
IngredientAmount% DV
Magnesium
mineralUNII · I38ZP9992A
UL · set6 effects
65 mg15%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
2.5 mg23%
Selenium
mineralUNII · H6241UJ22B
UL · set3 effects
9 mcg16%
Copper
mineralUNII · 789U1901C5
UL · set3 effects
0.35 mg39%
Chromium
mineralUNII · 0R0008Q3JB
1 effect
120 mcg343%
Vanadium
mineralUNII · 00J9J9XKDE
UL · set
8 mcg—
Proprietary Blend
Proprietary Blend (Combination)other
660 mg—
What this product supports · authorized claims

17 authority-backed effects

Rolled up from EFSA / FDA / NIH ODS authorized function claims on this product's active ingredients. Each row shows which ingredients contribute.

Flagged excipients

3 flagged · authority citations

  • ● AVOIDTitanium Dioxide
    color

    Banned in EU food products effective 2022-08 (Commission Regulation (EU) 2022/63) following EFSA Panel opinion that a safe daily intake could not be established due to genotoxicity concerns. Still GRAS in the US under 21 CFR 73.575 but EU position is stricter.

    eur-lex.europa.eu →efsa.europa.eu →ecfr.gov →
  • ◐ 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.

    eur-lex.europa.eu →
  • ◐ 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.

    fda.gov →federalregister.gov →
FDA CAERS · adverse event context
30
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

Hypromellose · Cellulose · Silicon Dioxide · Stearic Acid

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.