supplementhackr
Bausch & Lomb

PreserVision AREDS 2 Formula

Serving
2 Soft Gel(s)
Form
capsule-unknown
UPC
324208625040
DSLD
44503
Formula hash
5626aeea4fec
Brand context
Bausch & Lomb
CA
Catalog
47
products
With avoid flag
27
products
FDA recalls
0
history
CAERS
42
reports
Avoid-flaggedObjective label signals
Flagged excipients
2
1 avoid · 1 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
10 {Calories}—
Calories
otherUNII · 1
10 {Calories}—
Total Fat
Fat (unspecified)other
1 Gram(s)1%
Cholesterol
otherUNII · 97C5T2UQ7J
10 mg3%
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
226 mg337%
Vitamin E
vitaminUNII · H4N855PNZ1
UL · set1 effect
200 IU667%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
34.8 mg232%
Copper
mineralUNII · 789U1901C5
UL · set3 effects
0.8 mg40%
Omega-3 Fatty Acids
Omega-3fatty_acidUNII · 71M78END5S
1 effect
500 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

2 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 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).

    eur-lex.europa.eu →leginfo.legislature.ca.gov →
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