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GNC Men's

Staminol Ultra

Serving
2 Caplet(s)
Per container
30
Form
tablet
DSLD
243499
Formula hash
d1295ecdd881
Brand context
GNC Men's
Catalog
62
products
With avoid flag
25
products
FDA recalls
0
history
CAERS
4
reports
Avoid-flaggedObjective label signals
Flagged excipients
1
1 avoid · 0 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

17 active ingredients
IngredientAmount% DV
Vitamin E
vitaminUNII · H4N855PNZ1
UL · set1 effect
15 mg107%
Thiamine
ThiaminvitaminUNII · X66NSO3N35
3 effects
2 mg167%
Riboflavin
vitaminUNII · TLM2976OFR
5 effects
2 mg154%
Niacin
vitaminUNII · 2679MF687A
UL · set3 effects
25 mg156%
Folate
vitaminUNII · 935E97BOY8
UL · set2 effects
1000 mcg DFE250%
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
8 mcg333%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
17 mg155%
Selenium
mineralUNII · H6241UJ22B
UL · set3 effects
75 mcg136%
L-Arginine Hydrochloride
Arginineamino_acidUNII · F7LTH1E20Y
1000 mg—
Testofen Fenugreek seed extract
Fenugreekherb
600 mg—
MegaNatural-BP Grape seed extract
Grapeherb
300 mg—
Maca powder
Macaherb
100 mg—
Asian Ginseng Root Extract
Oriental GinsengherbUNII · CUQ3A77YXI
55 mg—
Yohimbe Bark Extract
YohimbeherbUNII · 9M051HS3S5
50 mg—
Horny Goat Weed extract
Epimediumherb
50 mg—
Hawthorn
herbUNII · 65ER808MP7
25 mg—
Ginkgo biloba Leaf Extract
GinkgoherbUNII · 19FUJ2C58T
LiverTox D
25 mg—
What this product supports · authorized claims

16 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

1 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 →
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

Microcrystaline Cellulose · Croscarmellose Sodium · Crospovidone · Hydroxypropylcellulose · Silica · Polyethylene Glycol · Stearic Acid · Talc · Magnesium Stearate