supplementhackr
Performix

SST v2X

Serving
1 Capsule(s)
Per container
30
Form
capsule-unknown
DSLD
273167
Formula hash
76d6867367dd
Brand context
Performix
Catalog
49
products
With avoid flag
12
products
FDA recalls
0
history
CAERS
14
reports
Caution-flaggedObjective label signals
Flagged excipients
4
0 avoid · 4 caution
FDA recalls
0
no recall history
CAERS reports
4
FDA consumer events
Certifications
0
none recorded
4 excipients carry authority-caution citations. · Every flag below links to the authority's published citation.

Supplement Facts

5 active ingredients
IngredientAmount% DV
Calories
otherUNII · 1
10 Calorie(s)—
Total Fat
Fat (unspecified)other
1 Gram(s)1%
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
1000 mcg41667%
Calories
otherUNII · 1
416 mg—
Calories
otherUNII · 1
896 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

  • ◐ CAUTIONFD&C Blue #1 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
    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 →
  • ◐ 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
4
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 · Sucrose · Starch · Pharmaceutical Glaze · Polyvinylpyrrolidone · Calcium Silicate · Maltodextrin