NutraChamps
Neura-Spark
Serving
1 Capsule(s)
Per container
30
Form
capsule-unknown
UPC
X001F4PE2F
DSLD
Formula hash
a52f7e14ff64
Catalog
143
products
With avoid flag
0
products
FDA recalls
0
history
CAERS
20
reports
Clean labelObjective label signals
Flagged excipients
0
none
FDA recalls
0
no recall history
CAERS reports
5
FDA consumer events
Certifications
0
none recorded
No authority-flagged excipients or recalls. · Every flag below links to the authority's published citation.
NIH LiverTox
2 ingredients with hepatotoxicity classification
Worst severity: Category D
- GinkgoCategory D
LiverTox Category D (hepatotoxicity — separate concern from IARC Group 2B carcinogenicity classification). A handful of hepatitis reports.
LiverTox → - St. John's WortCategory D
LiverTox Category D. Few case reports of hepatitis; causality uncertain. Major drug-interaction concern (CYP3A4 induction) — can reduce levels of warfarin, oral contraceptives, immunosuppressants, HIV antivirals.
LiverTox →
Supplement Facts
11 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Vitamin B12 vitaminUNII · 8406EY2OQA 3 effects | 500 mcg | 8330% |
| Bacopa monnieri BacopaherbUNII · DUB5K84ELI | 300 mg | — |
| Phosphatidylserine otherUNII · 394XK0IH40 | 125 mg | — |
| DMAE Deanolherb | 75 mg | — |
| Ginkgo biloba GinkgoherbUNII · 19FUJ2C58T LiverTox D | 50 mg | — |
| St. John's Wort extract St. John's WortherbUNII · UFH8805FKA LiverTox D | 50 mg | — |
| Acetyl L-Carnitine herbUNII · S3Z3R3X6RL | 50 mg | — |
| Gotu Kola extract Gotu Kolaherb | 50 mg | — |
| Rhodiola rosea Rhodiolaherb | 25 mg | — |
| L-Glutamine Glutamineamino_acidUNII · 0RH81L854J | 25 mg | — |
| Huperzine-A HuperzineherbUNII · 0111871I23 | 10 mcg | — |
What this product supports · authorized claims
3 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.
- from: Vitamin B12
- from: Vitamin B12
- from: Vitamin B12
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
Vegetable Cellulose Capsule