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Herbalife

Mega Garlic Plus

Serving
1 Tablet(s)
Per container
30
Form
tablet
UPC
0032
DSLD
2118
Formula hash
28131c899f7b
Brand context
Herbalife
Catalog
205
products
With avoid flag
32
products
FDA recalls
0
history
CAERS
1
reports
Avoid-flaggedObjective label signals
Flagged excipients
4
1 avoid · 3 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

5 active ingredients
IngredientAmount% DV
Total Carbohydrates
CarbohydrateotherUNII · 0
1 g1%
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
70 mg116%
Calcium
mineralUNII · SY7Q814VUP
UL · set6 effects
35 mg3%
Phosphorus
mineralUNII · 27YLU75U4W
UL · set2 effects
34 mg3%
Garlic powder
GarlicherbUNII · V1V998DC17
600 mg—
What this product supports · authorized claims

11 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

4 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 →
  • ◐ CAUTIONPropyl Paraben
    preservative

    EFSA 2004 re-evaluation (EFSA Journal 83) found propylparaben could not have an ADI established. EU banned propylparaben as food additive (Commission Regulation 1333/2008 Annex II removed it). US still permits.

    efsa.onlinelibrary.wiley.com →eur-lex.europa.eu →
  • ◐ CAUTIONFD&C Blue #1
    color

    EU requires 'attention in children' warning per Commission Regulation 1333/2008 Annex III. Limited to specific food categories; capsule-shell use permitted with restrictions.

    eur-lex.europa.eu →
  • ◐ 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 →
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 · Methacrylic Acid Copolymer · Croscarmellose Sodium · Hypromellose · Stearic Acid · Talc · Triethyl Citrate · Magnesium Stearate · Cellulose · Vegetable Acetoglycerides · Silicon Dioxide · Polyethylene Glycol · Polysorbate 80 · Methylparaben