Performix

Men's 8HR Time-Release Multi

Serving

2 Capsule(s)

Per container

Form

capsule-unknown

DSLD

268661

Avoid-flaggedObjective label signals

Flagged excipients

1 avoid · 2 caution

FDA recalls

no recall history

CAERS reports

FDA consumer events

Certifications

none recorded

1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

22 active ingredients

Ingredient	Amount	% DV
Vitamin A UNII · 81G40H8B0T	5000 IU	100%
Vitamin C UNII · PQ6CK8PD0R	60 mg	100%
Vitamin D UNII · 9VU1KI44GP	1000 IU	250%
Vitamin E UNII · H4N855PNZ1	30 IU	100%
Vitamin K UNII · A034SE7857	80 mcg	100%
Thiamine ThiaminUNII · X66NSO3N35	7.5 mg	500%
Riboflavin UNII · TLM2976OFR	8.5 mg	500%
Niacin UNII · 2679MF687A	20 mg	100%
Vitamin B6 UNII · KV2JZ1BI6Z	10 mg	500%
Folic Acid Vitamin B9 (folic acid)UNII · 935E97BOY8	800 mcg	200%
Vitamin B12 UNII · 8406EY2OQA	60 mcg	1000%
Biotin UNII · 6SO6U10H04	750 mcg	250%
Pantothenic Acid Pantothenic Acid (Vitamin B5)UNII · 19F5HK2737	10 mg	100%
Iron UNII · E1UOL152H7	9 mg	50%
Iodide IodineUNII · 09G4I6V86Q	150 mcg	100%
Zinc UNII · J41CSQ7QDS	15 mg	100%
Selenium UNII · H6241UJ22B	70 mcg	100%
Copper UNII · 789U1901C5	2 mg	100%
Manganese UNII · 42Z2K6ZL8P	2 mg	100%
Chromium UNII · 0R0008Q3JB	120 mcg	100%
Molybdenum UNII · 81AH48963U	75 mcg	100%
Men's Well-Being Blend Blend	1130 mg	—

Flagged excipients

3 flagged · authority citations

● AVOIDTitanium Dioxide
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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 Lake
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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 Lake
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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 →

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 · Talc · Dicalcium Phosphate · Sugar · Pharmaceutical Glaze · Silica · Povidone · Starch · Mannitol · Corn Oil · Tocopherols · Sodium Ascorbate