supplementhackr
Life

40+ Heart Defense

Serving
1 Capsule(s)
Per container
60
Form
capsule-unknown
UPC
860721000402
DSLD
82008
Formula hash
80a8b4b01dd1
Brand context
Life
Catalog
35
products
With avoid flag
1
products
FDA recalls
0
history
CAERS
12
reports
Avoid-flaggedObjective label signals
Flagged excipients
3
1 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
12
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
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
700 mg1167%
Moringa oleifera (leaf) powder
MoringaherbUNII · 4WET1AWO9B
25 mg—
Bryophyllum pinnatum
Kalanchoe pinnatumherb
25 mg—
Essential Amino Acids
Blend (Amino Acid/Protein)otherUNII · N7U7BXP2OI
0 NP—
Calories
otherUNII · 1
0 NP—
Calories
otherUNII · 1
0 NP—
Minerals
Blend (Combination)other
0 NP—
Calories
otherUNII · 1
0 NP—
Sugar
otherUNII · C151H8M554
0 NP—
What this product supports · authorized claims

5 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 #5
    color

    EU requires warning label 'may have an adverse effect on activity and attention in children' per Commission Regulation 1333/2008 Annex III (following Southampton study 2007). FDA requires specific label declaration (21 CFR 74.705).

    eur-lex.europa.eu →ecfr.gov →
  • ◐ CAUTIONFD&C Yellow #6
    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 →
FDA CAERS · adverse event context
12
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

Stearic Acid · Calcium Carbonate · Magnesium Stearate · Gelatin · FD & C Blue #1 · FD & C Red #40