Performix

SST V3X

Serving

2 Capsule(s)

Per container

Form

capsule-unknown

DSLD

275319

Formula hash

dbc7781ae9f1

Brand context

Performix

Catalog

products

With avoid flag

products

FDA recalls

history

CAERS

reports

Caution-flaggedObjective label signals

Flagged excipients

0 avoid · 3 caution

FDA recalls

no recall history

CAERS reports

FDA consumer events

Certifications

none recorded

3 excipients carry authority-caution citations. · Every flag below links to the authority's published citation.

Supplement Facts

5 active ingredients

Ingredient	Amount	% DV
Calories otherUNII · 1	10 Calorie(s)	—
Calories otherUNII · 1	1 Gram(s)	1%
Vitamin B12 vitaminUNII · 8406EY2OQA 3 effects	500 mcg	20833%
Performix SST Extreme Energy, Metabolism, Focus Terra Bead Complex Proprietary Blendother	530 mg	—
Calories otherUNII · 1	908 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.

↑Normal energy-yielding metabolism
from: Vitamin B12
EFSAEU-Reg-432/2012-ID-107 →
↑Normal formation of red blood cells + hemoglobin
from: Vitamin B12
EFSAEU-Reg-432/2012-ID-114 →LOINC 789-8
↓Normal homocysteine metabolism
from: Vitamin B12
EFSAEU-Reg-432/2012-ID-109 →LOINC 13965-9

Flagged excipients

3 flagged · authority citations

◐ CAUTIONFD&C Blue 2 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 →
◐ CAUTIONFD&C Red 40 Lake
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 Lake
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

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 · Sugar · Starch · Polyvinylpyrrolidone · Pharmaceutical Glaze · Cellulose · Potassium Aluminum Silicate