Rugby

Multilex

Serving
1 Tablet(s)
Form
tablet
UPC
005364044011
DSLD
Formula hash
dfd6e03c6d26
Brand context
Catalog
263
products
With avoid flag
96
products
FDA recalls
0
history
CAERS
11
reports
Avoid-flaggedObjective label signals
Flagged excipients
1
1 avoid · 0 caution
FDA recalls
0
no recall history
CAERS reports
7
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

16 active ingredients
IngredientAmount% DV
Vitamin A
vitaminUNII · 81G40H8B0T
UL · set3 effects
10000 IU200%
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
100 mg166%
Vitamin D3
Vitamin DvitaminUNII · 1C6V77QF41
UL · set4 effects
400 IU100%
Vitamin E
vitaminUNII · H4N855PNZ1
UL · set1 effect
5.5 IU18%
Thiamine
ThiaminvitaminUNII · X66NSO3N35
3 effects
10 mg666%
Riboflavin
vitaminUNII · TLM2976OFR
5 effects
5 mg294%
Niacinamide
NiacinvitaminUNII · 25X51I8RD4
UL · set3 effects
30 mg150%
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
1.7 mg85%
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
3 mcg50%
Pantothenic Acid
Pantothenic Acid (Vitamin B5)vitaminUNII · 19F5HK2737
10 mg100%
Iron
mineralUNII · E1UOL152H7
UL · set5 effects
15 mg83%
Iodine
mineralUNII · 9679TC07X4
UL · set2 effects
150 mcg100%
Magnesium
mineralUNII · I38ZP9992A
UL · set6 effects
5 mg2%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
1.5 mg10%
Copper
mineralUNII · 789U1901C5
UL · set3 effects
1 mg50%
Manganese
mineralUNII · 42Z2K6ZL8P
UL · set2 effects
1 mg50%
What this product supports · authorized claims

24 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.

FDA CAERS · adverse event context
7
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 · Croscarmellose Sodium · Stearic Acid · Vegetable Magnesium Stearate · Silicon Dioxide · Polydextrose · Hypromellose · Talc · Maltodextrin · Medium Chain Triglycerides · Caramel

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.