Superbalife International
Zyrexin 525 mg
Avoid-flaggedObjective label signals
Flagged excipients
2
1 avoid · 1 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
1 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Proprietary Herbal Blend Proprietary Blend (Herb/Botanical) | 1050 mg | — |
Flagged excipients
2 flagged · authority citations
- ● AVOIDTitanium Dioxidecolor
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.
- ◐ CAUTIONFD&C Blue #1 Aluminum Lakecolor
EU requires 'attention in children' warning per Commission Regulation 1333/2008 Annex III. Limited to specific food categories; capsule-shell use permitted with restrictions.
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
Microcrystalline Cellulose Dextrose · Starch · Stearic Acid · Hydroxy Propyl Methycellulose · Magnesium Stearate · Silica · Triacetin