Enzymatic Therapy

Healthy Cells Breast

Serving
1 Tablet(s)
Form
tablet
UPC
763948058761
DSLD
Formula hash
1d1597847146
Brand context
Catalog
675
products
With avoid flag
118
products
FDA recalls
0
history
CAERS
5
reports
Avoid-flaggedObjective label signals
Flagged excipients
1
1 avoid · 0 caution
FDA recalls
0
no recall history
CAERS reports
5
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.
NIH LiverTox
1 ingredient with hepatotoxicity classification
Worst severity: Category B
About LiverTox →
  • Green TeaCategory B

    LiverTox Category B (for concentrated extracts only, not brewed tea). High-dose EGCG (>800 mg/day) from supplements linked to hepatotoxicity. EFSA 2018 opinion. USP verification recommended.

    LiverTox →

Supplement Facts

10 active ingredients
IngredientAmount% DV
Total Carbohydrates
CarbohydrateotherUNII · 0
1 Gram(s)1%
Folate
vitaminUNII · 935E97BOY8
UL · set2 effects
200 mcg50%
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
500 mcg8333%
Calcium
mineralUNII · SY7Q814VUP
UL · set6 effects
50 mg5%
Iodine
mineralUNII · 9679TC07X4
UL · set2 effects
213 mcg142%
Calcium D-Glucarate
CalciummineralUNII · SST07NLK7J
UL · set6 effects
200 mg
Broccoli (Brassica oleracea) floret and stalk concentrate
BroccoliherbUNII · UOI4FT57BZ
125 mg
Green Tea (Camellia sinensis) leaf extract
Green TeaherbUNII · W2ZU1RY8B0
LiverTox B
50 mg
Maitake (Grifola frondosa) Mushroom
Maitake MushroomotherUNII · A1U5YJI0Z8
50 mg
Maitake (Grifola frondosa) Mushroom extract
Maitake MushroomotherUNII · A1U5YJI0Z8
5 mg
What this product supports · authorized claims

10 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

1 flagged · authority citations

  • ● AVOIDTitanium Dioxide color
    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.

FDA CAERS · adverse event context
5
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

Cellulose · Modified Cellulose · modified Cellulose Gum · Stearic Acid · Magnesium Stearate · Silicon Dioxide · Soy Lecithin · Carnauba Wax

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.