Pure Encapsulations
Nutrient 950 without iron
LNHPD
8089536
Formula hash
ad2d150a0c7b
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
9 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Vitamin B6 vitaminUNII · KV2JZ1BI6Z UL · set6 effects | 7.5 mg | — |
| Vitamin B6 vitaminUNII · KV2JZ1BI6Z UL · set6 effects | 7.5 mg | — |
| Inositol Hexanicotinate Inositol nicotinateherbUNII · 4L6452S749 | 15.0 mg | — |
| Iodine mineralUNII · 9679TC07X4 UL · set2 effects | 33.33 mcg | — |
| Molybdenum mineralUNII · 81AH48963U UL · set1 effect | 16.6 mcg | — |
| Zeaxanthin CarotenoidsherbUNII · C40H56O2 | 16.7 mcg | — |
| Manganese mineralUNII · 42Z2K6ZL8P UL · set2 effects | 0.83 mg | — |
| Copper mineralUNII · 789U1901C5 UL · set3 effects | 333.0 mcg | — |
| Lycopene herbUNII · SB0N2N0WV6 | 41.6 mcg | — |
What this product supports · authorized claims
12 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 B6
- from: Vitamin B6
- from: Copper · Vitamin B6
- from: Vitamin B6
- from: Copper
- from: Copper · Manganese
- from: Manganese
- from: Molybdenum
- from: Iodine
- from: Iodine
- from: Vitamin B6
- from: Vitamin B6
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 →