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Pure Encapsulations

Best-Rest Formula

Serving
2 Capsule(s)
Per container
60
Form
capsule-unknown
UPC
766298010960
DSLD
293903
Formula hash
70ffe0b60566
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 D
About LiverTox →
  • ValerianCategory D

    LiverTox Category D. A small number of published case reports of acute hepatitis associated with valerian supplements. Causality uncertain; concomitant hepatotoxic agents common.

    LiverTox →

Supplement Facts

9 active ingredients
IngredientAmount% DV
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
3.3 mg194%
Melatonin
otherUNII · JL5DK93RCL
1 mg—
Gamma-Aminobutyric Acid
GABAherbUNII · 2ACZ6IPC6I
300 mg—
Suntheanine
Theanineherb
50 mg—
Valerian Root Extract
ValerianherbUNII · JWF5YAW3QW
LiverTox D
400 mg—
Lemon Balm Leaf Extract
lemon balmherbUNII · 50D2ZE9219
150 mg—
Hops Aerial Parts Extract
Hopsherb
150 mg—
Passionflower Aerial Parts Extract
Passionflowerherb
100 mg—
Chamomile flower extract
Chamomile (unspecified)herbUNII · FGL3685T2X
100 mg—
What this product supports · authorized claims

6 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 · Plant Fiber · Gum Arabic · Maltodextrin · Ascorbyl Palmitate · Silica