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Generix Laboratories

Complex Phenylethylamine Provisional

Serving
1 Tablet(s)
Per container
60
Form
tablet
UPC
896025000206
DSLD
14437
Formula hash
b6ca4a93cdbb
Catalog
2
products
With avoid flag
2
products
FDA recalls
0
history
CAERS
0
reports
Avoid-flaggedObjective label signals
Flagged excipients
4
1 avoid · 3 caution
FDA recalls
0
no recall history
CAERS reports
0
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

2 active ingredients
IngredientAmount% DV
Niacin
vitaminUNII · 2679MF687A
UL · set3 effects
15 mg75%
BiphedAdrene 1(TM)
Proprietary Blend (non-nutrient/non-botanical)other
489 mg—
What this product supports · authorized claims

3 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

4 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 →
  • ◐ CAUTIONErythrosine Aluminum Lake
    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 Blue #1 Aluminum Lake
    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 Blue #2 Carmine Aluminum Lake
    color

    Banned from direct food use in Norway; restricted in EU under Commission Regulation 1333/2008. FDA permits under 21 CFR 74.102 with labeling requirement.

    eur-lex.europa.eu →
Other ingredients

Microcrystalline Cellulose · Stearic Acid · Magnesium Stearate · Silicon Dioxide · Croscarmellose Sodium · Polyvinyl Alcohol · Polyethylene Glycol · Talc