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Rugby

I-Vite Protect

Serving
2 Tablet(s)
Per container
60
Form
tablet
UPC
00536-4178-419
DSLD
14517
Formula hash
1df089431908
Brand context
Rugby
Catalog
263
products
With avoid flag
96
products
FDA recalls
0
history
CAERS
11
reports
Avoid-flaggedObjective label signals
Flagged excipients
3
1 avoid · 2 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

6 active ingredients
IngredientAmount% DV
Vitamin A
vitaminUNII · 81G40H8B0T
UL · set3 effects
14320 IU286%
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
226 mg376%
Vitamin E
vitaminUNII · H4N855PNZ1
UL · set1 effect
200 IU666%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
34.8 mg232%
Copper
mineralUNII · 789U1901C5
UL · set3 effects
0.8 mg40%
Sodium
mineralUNII · 9NEZ333N27
6 mg1%
What this product supports · authorized claims

14 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 #6 Lake
    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 →
  • ◐ CAUTIONFD&C Red #40 Lake
    color

    EU requires the same 'attention/activity in children' warning label as Yellow 5 per Commission Regulation 1333/2008 Annex III. California enacted a public-school ban effective 2028 (AB 2316, 2024).

    eur-lex.europa.eu →leginfo.legislature.ca.gov →
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 · Lactose · Gelatin · Dicalcium Phosphate · Croscarmellose Sodium · Hypromellose · Corn Starch · Silica · Stearic Acid · Polyvinylpyrrolidone · Magnesium Stearate · Talc · Triacetin · Glucose · Ethyl Vanillin · Sodium Ascorbate · Sodium Benzoate · tocopherols · Sorbic Acid · Polyethylene Glycol

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.