Bausch & Lomb

Ocuvite Adult 50+

Serving
1 Softgel(s)
Form
capsule-unknown
UPC
324208465707
DSLD
Formula hash
3435759ec7ac
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

11 active ingredients
IngredientAmount% DV
Calories
otherUNII · 1
5 Calorie(s)
Calories
otherUNII · 1
5 Calorie(s)
Total Fat
Fat (unspecified)other
0.5 Gram(s)1%
Cholesterol
otherUNII · 97C5T2UQ7J
5 mg2%
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
150 mg250%
Vitamin E
vitaminUNII · H4N855PNZ1
UL · set1 effect
30 IU100%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
9 mg60%
Copper
mineralUNII · 789U1901C5
UL · set3 effects
1 mg50%
Omega-3 Fatty Acids
Omega-3fatty_acidUNII · 71M78END5S
1 effect
250 mg
Lutein
herbUNII · X72A60C9MT
5 mg
Zeaxanthin
CarotenoidsherbUNII · C40H56O2
1 mg
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.

  • ◐ CAUTIONFD&C Red #40
    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).

  • ◐ 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.

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

Gelatin · Fish Oil · Glycerin · yellow Beeswax · Silicon Dioxide · Soy Lecithin · Natural flavoring

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.