Alcon

I-Caps AREDS Formula

Serving
1 Softgel(s)
Per container
60
Form
capsule-unknown
UPC
300658046031
DSLD
Formula hash
78630c2de2bc
Brand context
Catalog
20
products
With avoid flag
15
products
FDA recalls
0
history
CAERS
2
reports
Avoid-flaggedObjective label signals
Flagged excipients
3
1 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
2
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

9 active ingredients
IngredientAmount% DV
Calories
otherUNII · 1
5 {Calories}
Total Fat
Fat (unspecified)other
0.5 Gram(s)0.6%
Total Carbohydrates
CarbohydrateotherUNII · 0
0.5 Gram(s)1%
Protein
Protein (unspecified)other
0.2 Gram(s)1%
Vitamin A
vitaminUNII · 81G40H8B0T
UL · set3 effects
14320 IU286%
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
226 mg377%
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%
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 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).

  • ◐ 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
2
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 · Glycerin · Soybean Oil · Coconut Oil · Corn Oil · Lecithin · Vegetable Glycerides · Beeswax · Polyunsaturated Oils · Caramel · Oxalic Acid · Metal Salts · DL-Alpha-Tocopherol · Cuprous Oxide

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.