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ALLMAX

Immunocharge

Serving
2 Tablet(s)
Per container
30
Form
tablet
UPC
665553200859
DSLD
326017
Avoid-flaggedObjective label signals
Flagged excipients
3
1 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
0
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 C
About LiverTox →
  • TurmericCategory C

    LiverTox Category C. 2020-2024 rise in acute liver injury cases linked specifically to high-dose concentrated turmeric/curcumin extracts with enhanced-bioavailability formulations (piperine, phospholipid complex). Not associated with culinary use.

    LiverTox →

Supplement Facts

16 active ingredients
IngredientAmount% DV
Vitamin A
UNII · 81G40H8B0T
1500 mcg RAE167%
Vitamin C
UNII · PQ6CK8PD0R
350 mg389%
Vitamin E
UNII · H4N855PNZ1
64 mg424%
Calcium
UNII · SY7Q814VUP
350 mg27%
Zinc
UNII · J41CSQ7QDS
10 mg91%
Selenium
UNII · H6241UJ22B
30 mcg55%
L-Glutamine
GlutamineUNII · 0RH81L854J
100 mg—
Milk Thistle Seed Extract Concentrate
Milk Thistle
100 mg—
American Ginseng root extract
American GinsengUNII · 8W75VCV53Q
94 mg—
Red Wine Fruit Extract
Red Wine
40 mg—
Pomegranate extract
PomegranateUNII · 56687D1Z4D
33 mg—
Grape Seed Extract Concentrate
Grape
25 mg—
Turmeric root powder
TurmericUNII · 856YO1Z64F
25 mg—
Alpha Lipoic Acid
UNII · 73Y7P0K73Y
25 mg—
Silicon Dioxide
SiliconUNII · ETJ7Z6XBU4
20 mg—
Coenzyme Q10
10 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

3 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 →
  • ◐ CAUTIONFD&C Yellow #5
    color

    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 →
  • ◐ CAUTIONFD&C Yellow #6
    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 →
Other ingredients

Microcrystalline Cellulose · Croscarmellose Sodium · Stearic Acid · Magnesium Stearate · Sodium Citrate · Polyvinyl Alcohol · Macrogol · Talc