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BSN

Nitrix

Serving
3 Tablet(s)
Per container
10
Form
tablet
UPC
834266010134
DSLD
30770
Formula hash
a36a5d6ee8a4
Brand context
BSN
Catalog
224
products
With avoid flag
9
products
FDA recalls
0
history
CAERS
6
reports
Avoid-flaggedObjective label signals
Flagged excipients
4
1 avoid · 3 caution
FDA recalls
0
no recall history
CAERS reports
6
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
12 mg60%
NITRIX(R) 2.0 PROPRIETARY BLEND
Proprietary Blend (Combination)other
3.6 Gram(s)—
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 →
  • ◐ 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 →
  • ◐ CAUTIONFD&C Blue #2
    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 →
FDA CAERS · adverse event context
6
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

Aqueous Coating · Microcrystalline Cellulose · Stearic Acid · Croscarmellose Sodium · Magnesium Stearate · Silicon Dioxide

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.