Genuine Health
greens+ daily dx
LNHPD
4079946
Formula hash
612b219ca75f
Catalog
148
products
With avoid flag
0
products
FDA recalls
0
history
CAERS
1
reports
Clean labelObjective label signals
Flagged excipients
0
none
FDA recalls
0
no recall history
CAERS reports
1
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
1 ingredient 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 →
Supplement Facts
16 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Triticum aestivum other | 383.0 mg | — |
| Cynara scolymus other | 100.0 mg | — |
| Lactobacillus casei otherUNII · SA940P2U00 | 0.09 billion cfu | — |
| Lactobacillus helveticus otherUNII · Q08Z44662J | 0.19 billion cfu | — |
| Palmaria palmata other | 33.0 mg | — |
| Camellia sinensis herb | 15.0 mg | — |
| Lactobacillus plantarum otherUNII · QFC21096ON | 0.09 billion cfu | — |
| Vitamin C vitaminUNII · PQ6CK8PD0R UL · set5 effects | 250.0 mg | — |
| Fructooligosaccharides Fructo-Oligosaccharides (FOS)otherUNII · 8LLD82AE3S | 100.0 mg | — |
| Lecithin lecithinotherUNII · H1109Z9J4N | 2171.0 mg | — |
| Ginkgo biloba GinkgoherbUNII · 19FUJ2C58T LiverTox D | 20.0 mg | — |
| Ginkgo biloba GinkgoherbUNII · 19FUJ2C58T LiverTox D | — | — |
| Bifidobacterium longum otherUNII · 831AQW699W | 0.04 billion cfu | — |
| Camellia sinensis herb | 15.0 mg | — |
| Malus domestica other | 1033.0 mg | — |
| Aminoacetic acid other | 500.0 mg | — |
What this product supports · authorized claims
5 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 C
- from: Vitamin C
- from: Vitamin C
- from: Vitamin C
- from: Vitamin C
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 →