Pure Encapsulations
Ultranutrient
LNHPD
20977710
Formula hash
6c5ed0e9fef7
Brand context
Catalog
2,199
products
With avoid flag
0
products
FDA recalls
2
history
CAERS
14
reports
Recall historyObjective label signals
Flagged excipients
0
none
FDA recalls
2
2 Class I / II
CAERS reports
9
FDA consumer events
Certifications
0
none recorded
2 FDA recalls on file. · Every flag below links to the authority's published citation.
Supplement Facts
10 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Biotin vitaminUNII · 6SO6U10H04 3 effects | 133.3 micrograms | — |
| (3R,3'R,6'R)-beta,epsilon-Carotene-3,3'-diol other | 141.6 micrograms | — |
| all-trans-beta-Carotene-3,3'-diol other | 8.5 micrograms | — |
| L-Glutathione GluthathioneherbUNII · GAN16C9B8O | 8.3 milligrams | — |
| Folate vitaminUNII · 935E97BOY8 UL · set2 effects | 133.3 micrograms | — |
| Vitamin C vitaminUNII · PQ6CK8PD0R UL · set5 effects | 6.72 milligrams | — |
| Crataegus monogyna other | 16.6 milligrams | — |
| Molybdenum mineralUNII · 81AH48963U UL · set1 effect | 16.6 micrograms | — |
| 3-Pyridinecarboxamide other | 16.6 mg | — |
| Zingiber officinale Gingerherb | 16.6 milligrams | — |
What this product supports · authorized claims
11 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
- from: Vitamin C
- from: Vitamin C
- from: Vitamin C
- from: Biotin
- from: Biotin
- from: Biotin
- from: Molybdenum
- from: Folate
- from: Vitamin C
- from: Vitamin C
Recall history
2 FDA recalls
- Class III2017-11-17brand-level
Pure Encapsulations Systemic Enzyme Complex DIETARY SUPPLEMENT 180 CAPSULES UPC: 7 66298 00862 2
Reason: Product contains undeclared sulfites.
FDA record → - Class III2017-11-17brand-level
pure encapsulations AI Enzymes DIETARY SUPPLEMENT 120 CAPSULES UPC: 7 66298 00318 4 and 60 CAPSULES UPC: 7 66298 00317 7
Reason: Product contains undeclared sulfites.
FDA record →
FDA CAERS · adverse event context
9
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 →