Metagenics
Ultra IX 360 Orange
LNHPD
22416849
Formula hash
192cb21350bd
Catalog
1,340
products
With avoid flag
1
products
FDA recalls
0
history
CAERS
4
reports
Clean labelObjective label signals
Flagged excipients
0
none
FDA recalls
0
no recall history
CAERS reports
3
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 | 100.0 mcg | — |
| Vitamin D vitaminUNII · 9VU1KI44GP UL · set4 effects | 5.0 mcg | — |
| 3,3',4',5,7-pentahydroxyflavone other | 100.0 mg | — |
| Selenium mineralUNII · H6241UJ22B UL · set3 effects | 26.25 mcg | — |
| Chromium mineralUNII · 0R0008Q3JB 1 effect | 60.0 mcg | — |
| Vitamin B12 vitaminUNII · 8406EY2OQA 3 effects | 1.5 mcg | — |
| Vitamin A vitaminUNII · 81G40H8B0T UL · set3 effects | 187.7 mcg RAE | — |
| Calcium mineralUNII · SY7Q814VUP UL · set6 effects | 250.0 mg | — |
| Copper mineralUNII · 789U1901C5 UL · set3 effects | 0.75 mg | — |
| Iodine mineralUNII · 9679TC07X4 UL · set2 effects | 18.75 mcg | — |
| L-Glutamine Glutamineamino_acidUNII · 0RH81L854J | 375.0 mg | — |
| Biotin vitaminUNII · 6SO6U10H04 3 effects | 37.5 mcg | — |
What this product supports · authorized claims
20 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: Folate · Vitamin B12
- from: Biotin · Calcium · Vitamin B12
- from: Calcium · Vitamin D
- from: Calcium · Vitamin D
- from: Calcium
- from: Calcium
- from: Calcium
- from: Copper · Selenium · Vitamin A · Vitamin D
- from: Iodine · Selenium
- from: Vitamin D
- from: Chromium
- from: Vitamin A
- from: Vitamin A
- from: Copper
- from: Copper
- from: Biotin
- from: Biotin
- from: Iodine
- from: Folate · Vitamin B12
- from: Selenium
FDA CAERS · adverse event context
3
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 →