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Peptiva

Peptiva + Sleep Support

Serving
1 Vegetarian Capsule(s)
Per container
30
Form
capsule-unknown
UPC
855710002512
DSLD
178248
Formula hash
aa2ad574217e
Brand context
Peptiva
Catalog
6
products
With avoid flag
4
products
FDA recalls
0
history
CAERS
1
reports
Avoid-flaggedObjective label signals
Flagged excipients
3
1 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
1
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

5 active ingredients
IngredientAmount% DV
Proprietary Probiotic Matrix
Proprietary Blend (Metabolite, constituent, extract, isolate, or combination of these)other
0 NP—
Gamma-Aminobutyric Acid
GABAherbUNII · 2ACZ6IPC6I
100 mg—
Valerian Root Extract
ValerianherbUNII · JWF5YAW3QW
LiverTox D
50 mg—
Melatonin
otherUNII · JL5DK93RCL
0.75 mg—
Melatonin
otherUNII · JL5DK93RCL
0.75 mg—
Flagged excipients

3 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 →
  • ◐ CAUTIONFD&C Red #40
    color

    EU requires the same 'attention/activity in children' warning label as Yellow 5 per Commission Regulation 1333/2008 Annex III. California enacted a public-school ban effective 2028 (AB 2316, 2024).

    eur-lex.europa.eu →leginfo.legislature.ca.gov →
  • ◐ CAUTIONFD&C Blue #1
    color

    EU requires 'attention in children' warning per Commission Regulation 1333/2008 Annex III. Limited to specific food categories; capsule-shell use permitted with restrictions.

    eur-lex.europa.eu →
FDA CAERS · adverse event context
1
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

Hypromellose · Microcrystalline Cellulose · Maltodextrin · Silica · Starch · Magnesium Stearate

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.