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GNC Men's

ArginMax

Serving
3 Caplet(s)
Per container
15
UPC
048107042936
DSLD
315301
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.
NIH LiverTox
1 ingredient with hepatotoxicity classification
Worst severity: Category D
About LiverTox →
  • GinkgoCategory D

    LiverTox Category D (hepatotoxicity — separate concern from IARC Group 2B carcinogenicity classification). A handful of hepatitis reports.

    LiverTox →

Supplement Facts

19 active ingredients
IngredientAmount% DV
Calories
UNII · 1
5 Calorie(s)—
Total Carbohydrates
CarbohydrateUNII · 0
2 Gram(s)1%
Vitamin A
UNII · 81G40H8B0T
5000 IU100%
Vitamin C
UNII · PQ6CK8PD0R
60 mg100%
Vitamin E
UNII · H4N855PNZ1
30 IU100%
Thiamine
ThiaminUNII · X66NSO3N35
1.5 mg100%
Riboflavin
UNII · TLM2976OFR
1.7 mg100%
Niacin
UNII · 2679MF687A
20 mg100%
Vitamin B6
UNII · KV2JZ1BI6Z
2 mg100%
Folate
UNII · 935E97BOY8
400 mcg100%
Vitamin B12
UNII · 8406EY2OQA
6 mcg100%
Biotin
UNII · 6SO6U10H04
300 mcg100%
Pantothenic Acid
Pantothenic Acid (Vitamin B5)UNII · 19F5HK2737
10 mg100%
Zinc
UNII · J41CSQ7QDS
15 mg100%
Selenium
UNII · H6241UJ22B
70 mcg100%
L-Arginine
ArginineUNII · 94ZLA3W45F
3 Gram(s)—
Asian Ginseng Aerial Parts, Root Extract
Ginseng
100 mg—
American Ginseng
UNII · 8W75VCV53Q
100 mg—
Ginkgo biloba
GinkgoUNII · 19FUJ2C58T
50 mg—
What this product supports · authorized claims

18 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

Cellulose · Calcium Carbonate · Acetoglycerides