NDS Nutrition

Neuro Sphere

Serving
3 Capsule(s)
Per container
30
Form
capsule-unknown
DSLD
Formula hash
c279d04ade4e
Brand context
Catalog
24
products
With avoid flag
10
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 →
  • GinkgoCategory D

    LiverTox Category D (hepatotoxicity — separate concern from IARC Group 2B carcinogenicity classification). A handful of hepatitis reports.

    LiverTox →

Supplement Facts

9 active ingredients
IngredientAmount% DV
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
1000 mcg41667%
Memory Cognition Blend
Blendother
1480 mg
Alpha Glycerophosphocholine
Alpha-GPCherb
250 mg
Ginkgo biloba
GinkgoherbUNII · 19FUJ2C58T
LiverTox D
180 mg
Huperzine-A
HuperzineherbUNII · 0111871I23
10 mcg
Mental Relaxation Blend
Blendother
500 mg
Mental Stimulant Time-Release Blend
Blendother
150 mg
Zum-Release Blend
Caffeineherb
50 mg
ZumXR DR Caffeine
Caffeineherb
0 NP
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.

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.

  • ◐ CAUTIONFD&C Yellow 6
    color

    EU requires 'attention in children' warning per Reg 1333/2008 Annex III (Southampton study 2007). Banned in Norway + Finland; allowed in US under 21 CFR 74.706 with declaration.

  • ◐ CAUTIONFD&C Red 3
    color

    FDA revoked food/ingested-drug color additive approval for FD&C Red 3 in January 2025 (Docket FDA-2022-C-2886). Manufacturers have until January 2027 (foods) / January 2028 (ingested drugs) to reformulate.

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

Gelatin · Vegetable Stearate · Silicon Dioxide · Rice Flour