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Trigen Laboratories

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Serving
1 Capsule(s)
Per container
60
Form
capsule-unknown
UPC
313811528602
DSLD
264480
Formula hash
a75c0ca53b82
Brand context
Trigen Laboratories
Catalog
38
products
With avoid flag
23
products
FDA recalls
0
history
CAERS
1
reports
Avoid-flaggedObjective label signals
Flagged excipients
3
1 avoid · 2 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

5 active ingredients
IngredientAmount% DV
Total Carbohydrates
CarbohydrateotherUNII · 0
240 mg—
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
15 mcg250%
elemental Iron
IronmineralUNII · E1UOL152H7
5 effects
2.4× ULexceeds NIH ODS adult upper limitsource →
110 mg611%
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
75 mg125%
Folate
vitaminUNII · 935E97BOY8
UL · set2 effects
0.5 mg125%
What this product supports · authorized claims

10 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 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 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 →
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

Microcrystalline Cellulose · Gelatin · fumed Silica · Magnesium Stearate · Tripotassium Citrate · Citric Acid