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Pure Encapsulations

DopaPlus

Serving
3 Capsule(s)
Per container
60
Form
capsule-unknown
UPC
766298014555
DSLD
309484
Formula hash
83ad655f5a0e
Brand context
Pure Encapsulations
Catalog
2,199
products
With avoid flag
0
products
FDA recalls
2
history
CAERS
14
reports
Recall historyObjective label signals
Flagged excipients
0
none
FDA recalls
2
2 Class I / II
CAERS reports
9
FDA consumer events
Certifications
0
none recorded
2 FDA recalls on file. · 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

8 active ingredients
IngredientAmount% DV
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
6.7 mg394%
Metafolin
Folatevitamin
UL · set2 effects
833 mcg DFE208%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
10 mg91%
L-Tyrosine
Tyrosineamino_acidUNII · 42HK56048U
1000 mg—
Velvet Bean Seed Extract
Cowhageherb
200 mg—
Rhodiola Root Extract
RhodiolaherbUNII · 3S5ITS5ULN
100 mg—
Grape seed extract
GrapeherbUNII · C34U15ICXA
100 mg—
Green Tea (Camellia sinensis) leaf extract
Green TeaherbUNII · W2ZU1RY8B0
LiverTox B
100 mg—
What this product supports · authorized claims

13 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.

Recall history

2 FDA recalls

  1. Class III2017-11-17brand-level

    Pure Encapsulations Systemic Enzyme Complex DIETARY SUPPLEMENT 180 CAPSULES UPC: 7 66298 00862 2

    Reason: Product contains undeclared sulfites.

    FDA record →
  2. Class III2017-11-17brand-level

    pure encapsulations AI Enzymes DIETARY SUPPLEMENT 120 CAPSULES UPC: 7 66298 00318 4 and 60 CAPSULES UPC: 7 66298 00317 7

    Reason: Product contains undeclared sulfites.

    FDA record →
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

Cellulose · Water