Genuine Health
Multi+ daily bone builder
LNHPD
5289882
Formula hash
39e3f174b56d
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
12 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Folate vitaminUNII · 935E97BOY8 UL · set2 effects | 125.0 mcg | — |
| Thiamine ThiaminvitaminUNII · X66NSO3N35 3 effects | 7.5 mg | — |
| Vitamin D vitaminUNII · 9VU1KI44GP UL · set4 effects | 5.0 mcg | — |
| Vitamin E vitaminUNII · H4N855PNZ1 UL · set1 effect | 17.0 mg AT | — |
| Beta-Carotene Vitamin AvitaminUNII · 01YAE03M7J UL · set3 effects | 37.5 mcg RAE | — |
| Beta-Carotene Vitamin AvitaminUNII · 01YAE03M7J UL · set3 effects | 75.0 mcg | — |
| Molybdenum mineralUNII · 81AH48963U UL · set1 effect | 12.5 mcg | — |
| Iodine mineralUNII · 9679TC07X4 UL · set2 effects | 50.0 mcg | — |
| Vitamin K2 Vitamin K (menaquinone)vitaminUNII · 71ANL51TLA | 60.0 mcg | — |
| Boron mineralUNII · N9E3X5056Q UL · set | 300.0 mcg | — |
| Vitamin C vitaminUNII · PQ6CK8PD0R UL · set5 effects | 50.0 mg | — |
| Riboflavin vitaminUNII · TLM2976OFR 5 effects | 25.0 mg | — |
What this product supports · authorized claims
18 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: Riboflavin · Thiamin
- from: Riboflavin · Thiamin
- from: Thiamin
- from: Riboflavin · Vitamin A
- from: Folate
- from: Vitamin D
- from: Vitamin D
- from: Vitamin A · Vitamin C · Vitamin D
- from: Vitamin D
- from: Vitamin A
- from: Vitamin C
- from: Vitamin C
- from: Molybdenum
- from: Iodine
- from: Iodine
- from: Riboflavin · Vitamin C · Vitamin E
- from: Riboflavin · Vitamin C
- from: Folate
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 →