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Enzymatic Therapy

Relax-O-Zyme

Serving
2 Tablet(s)
Per container
45
Form
tablet
UPC
763948020591
DSLD
39142
Formula hash
b319dd850960
Brand context
Enzymatic Therapy
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 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

10 active ingredients
IngredientAmount% DV
Total Carbohydrates
CarbohydrateotherUNII · 0
1 Gram(s)1%
Vitamin D
vitaminUNII · 9VU1KI44GP
UL · set4 effects
100 IU26%
Niacin
vitaminUNII · 2679MF687A
3 effects
3.7× ULexceeds NIH ODS adult upper limitsource →
130 mg650%
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
20 mg1000%
Calcium
mineralUNII · SY7Q814VUP
UL · set6 effects
90 mg9%
Magnesium
mineralUNII · I38ZP9992A
UL · set6 effects
105 mg26%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
5 mg33%
Valerian Root Extract
ValerianherbUNII · JWF5YAW3QW
LiverTox D
150 mg—
Hops Flower Extract
HopsherbUNII · 01G73H6H83
60 mg—
Passionflower (aerial parts) powder
Passionflowerherb
60 mg—
What this product supports · authorized claims

19 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.

    eur-lex.europa.eu →efsa.europa.eu →ecfr.gov →
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 Gum · Stearic Acid · Modified Cellulose · Polydextrose · Magnesium Stearate · Silicon Dioxide · Maltodextrin · Medium Chain Triglycerides · Anise · Peppermint