supplementhackr
Trigen Laboratories

TL-Select DHA

Serving
1 Softgel Capsule(s)
Per container
30
Form
capsule-unknown
UPC
313811507300
DSLD
264482
Avoid-flaggedObjective label signals
Flagged excipients
4
1 avoid · 3 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

10 active ingredients
IngredientAmount% DV
Vitamin C
UNII · PQ6CK8PD0R
28 mg47%
Vitamin D
UNII · 9VU1KI44GP
800 IU200%
Vitamin D3
Vitamin DUNII · 1C6V77QF41
30 IU100%
Vitamin B6
UNII · KV2JZ1BI6Z
25 mg1000%
Folate
UNII · 935E97BOY8
1.25 mg156%
Biotin
UNII · 6SO6U10H04
250 mcg83%
Calcium
UNII · SY7Q814VUP
160 mg12%
Iron
UNII · E1UOL152H7
29 mg161%
Fish Oil Blend
Blend (Fatty Acid or Fat/Oil Supplement)
660 mg—
Docusate Calcium
Docusate calcium
55 mg4%
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 →
  • ◐ 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 #5
    color

    EU requires warning label 'may have an adverse effect on activity and attention in children' per Commission Regulation 1333/2008 Annex III (following Southampton study 2007). FDA requires specific label declaration (21 CFR 74.705).

    eur-lex.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 →
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 · Glycerin · Soy Lecithin · Beeswax · Water · Sorbitol · Sorbitan