Bausch & Lomb

Ocuvite With Lutein

Serving
1 Tablet(s)
Form
tablet
UPC
324208387603
DSLD
Formula hash
be5f6c88c2f4
Brand context
CA
Catalog
47
products
With avoid flag
27
products
FDA recalls
0
history
CAERS
42
reports
Avoid-flaggedObjective label signals
Flagged excipients
3
1 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
9
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

7 active ingredients
IngredientAmount% DV
Vitamin A
vitaminUNII · 81G40H8B0T
UL · set3 effects
1000 IU20%
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
200 mg333%
Vitamin E
vitaminUNII · H4N855PNZ1
UL · set1 effect
60 IU200%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
40 mg267%
Selenium
mineralUNII · H6241UJ22B
UL · set3 effects
55 mcg79%
Copper
mineralUNII · 789U1901C5
UL · set3 effects
2 mg100%
Lutein
herbUNII · X72A60C9MT
2 mg
What this product supports · authorized claims

15 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.

  • ◐ CAUTIONFD&C Yellow #6 Dye
    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.

  • ◐ 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.

FDA CAERS · adverse event context
9
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

Dibasic Calcium Phosphate · Microcrystalline Cellulose · Hypromellose · Crospovidone · Magnesium Stearate · Silicon Dioxide · Stearic Acid · Triethyl Citrate · Polysorbate 80

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.