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GNC Women's

Phytoestrogen Formula

Serving
2 Softgel Capsule(s)
Per container
30
Form
capsule-unknown
UPC
048107136970
DSLD
74755
Formula hash
fc66ab504c29
Brand context
GNC Women's
Catalog
174
products
With avoid flag
103
products
FDA recalls
0
history
CAERS
6
reports
Avoid-flaggedObjective label signals
Flagged excipients
1
1 avoid · 0 caution
FDA recalls
0
no recall history
CAERS reports
3
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 C
About LiverTox →
  • Black CohoshCategory C

    LiverTox Category C. 40+ published case reports of acute liver injury. EMA HMPC 2010 monograph requires warning label in EU. FDA advisory encourages caution.

    LiverTox →

Supplement Facts

9 active ingredients
IngredientAmount% DV
Calories
otherUNII · 1
15 Calorie(s)—
Total Fat
Fat (unspecified)other
1.5 Gram(s)2%
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
50 mg2500%
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
100 mcg1667%
Calcium
mineralUNII · SY7Q814VUP
UL · set6 effects
200 mg20%
Magnesium
mineralUNII · I38ZP9992A
UL · set6 effects
100 mg25%
Evening Primrose Oil
Evening Primrose oilotherUNII · 3Q9L08K71N
300 mg—
Black Cohosh Root Extract
Black CohoshherbUNII · K73E24S6X9
LiverTox C
40 mg—
Soy Isoflavone Extract
Soyherb
125 mg—
What this product supports · authorized claims

12 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

    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 →
FDA CAERS · adverse event context
3
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

Soybean Oil · Gelatin · Glycerin · Caramel color

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.