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VitaliKoR

VitaliKoR:Test

Serving
2 Capsule(s)
Per container
30
Form
capsule-unknown
DSLD
31973
Formula hash
2e73aebecc2b
Brand context
VitaliKoR
Catalog
8
products
With avoid flag
1
products
FDA recalls
0
history
CAERS
4
reports
Avoid-flaggedObjective label signals
Flagged excipients
6
1 avoid · 5 caution
FDA recalls
0
no recall history
CAERS reports
1
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

11 active ingredients
IngredientAmount% DV
Proprietary Blend
Proprietary Blend (Combination)other
754 mg—
Magnesium (Citrate)
MagnesiummineralUNII · RHO26O1T9V
UL · set6 effects
22 mg5.5%
Trigonella foenum-graecum
FenugreekherbUNII · 9H95SL7TEV
0 Not Present—
Apple extract
AppleherbUNII · B423VGH5S9
0 Not Present—
Rhodiola Rosea 5/2
Rhodiolaherb
0 Not Present—
Rhaponticum carthamoides
Maral Rootherb
0 Not Present—
Grape extract
GrapeherbUNII · 3GOV20705G
0 Not Present—
Boron Aminomin
Boronherb
UL · set
0 Not Present—
Zinc Citrate
ZincmineralUNII · K72I3DEX9B
UL · set8 effects
9 mg60%
PhytoForce(R) delivery system
Proprietary Blend (Combination)other
0 Not Present—
Black Pepper extract
Black PepperherbUNII · KM66971LVF
0 Not Present—
What this product supports · authorized claims

13 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

6 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 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.

    ecfr.gov →
  • ◐ 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 →
  • ◐ 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).

    eur-lex.europa.eu →leginfo.legislature.ca.gov →
  • ◐ 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.

    eur-lex.europa.eu →
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

Rice Flour powder · Magnesium Stearate · Silica · Gelatin