Genuine Health
multi+ daily glow
LNHPD
4605432
Formula hash
356d2a6a0ccb
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.
Supplement Facts
14 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Vitis vinifera Grapeherb | 12.5 mg | — |
| Vitis vinifera Grapeherb | — | — |
| Chromium mineralUNII · 0R0008Q3JB 1 effect | 100.0 mcg | — |
| Selenium mineralUNII · H6241UJ22B UL · set3 effects | 25.0 mcg | — |
| Thiamine ThiaminvitaminUNII · X66NSO3N35 3 effects | 12.5 mg | — |
| Manganese mineralUNII · 42Z2K6ZL8P UL · set2 effects | 1.0 mg | — |
| Calcium mineralUNII · SY7Q814VUP UL · set6 effects | 50.0 mg | — |
| Calcium mineralUNII · SY7Q814VUP UL · set6 effects | 50.0 mg | — |
| Copper mineralUNII · 789U1901C5 UL · set3 effects | 500.0 mcg | — |
| Iodine mineralUNII · 9679TC07X4 UL · set2 effects | 50.0 mcg | — |
| Vanadium mineralUNII · 00J9J9XKDE UL · set | 12.5 mcg | — |
| Molybdenum mineralUNII · 81AH48963U UL · set1 effect | 12.5 mcg | — |
| Punica granatum Pomegranateherb | 25.0 mg | — |
| Vitamin B6 vitaminUNII · KV2JZ1BI6Z UL · set6 effects | 12.5 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.
- from: Calcium · Thiamin · Vitamin B6
- from: Thiamin · Vitamin B6
- from: Thiamin
- from: Copper · Selenium · Vitamin B6
- from: Vitamin B6
- from: Calcium · Manganese
- from: Calcium
- from: Calcium
- from: Calcium
- from: Calcium
- from: Iodine · Selenium
- from: Chromium
- from: Copper
- from: Copper · Manganese
- from: Molybdenum
- from: Iodine
- from: Vitamin B6
- from: Vitamin B6
- from: Selenium
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 →