Pure Encapsulations
Nutrient 950
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
26 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Vitamin A UNII · 81G40H8B0T | 7500 IU | 150% |
| Vitamin C UNII · PQ6CK8PD0R | 500 mg | 833% |
| Vitamin D UNII · 9VU1KI44GP | 400 IU | 100% |
| Vitamin E UNII · H4N855PNZ1 | 200 IU | 667% |
| Thiamine ThiaminUNII · X66NSO3N35 | 50 mg | 3333% |
| Riboflavin UNII · TLM2976OFR | 34.75 mg | 2044% |
| Niacin UNII · 2679MF687A | 86 mg | 430% |
| Vitamin B6 UNII · KV2JZ1BI6Z | 20.5 mg | 1025% |
| Folate UNII · 935E97BOY8 | 400 mcg | 100% |
| Vitamin B12 UNII · 8406EY2OQA | 500 mcg | 8333% |
| Biotin UNII · 6SO6U10H04 | 400 mcg | 133% |
| Pantothenic Acid Pantothenic Acid (Vitamin B5)UNII · 19F5HK2737 | 200 mg | 2000% |
| Calcium UNII · SY7Q814VUP | 150 mg | 15% |
| Iron UNII · E1UOL152H7 | 5 mg | 28% |
| Iodine UNII · 9679TC07X4 | 100 mcg | 67% |
| Magnesium UNII · I38ZP9992A | 100 mg | 25% |
| Zinc UNII · J41CSQ7QDS | 12.5 mg | 83% |
| Selenium UNII · H6241UJ22B | 100 mcg | 143% |
| Copper UNII · 789U1901C5 | 1 mg | 50% |
| Manganese UNII · 42Z2K6ZL8P | 2.5 mg | 125% |
| Chromium UNII · 0R0008Q3JB | 100 mcg | 83% |
| Molybdenum UNII · 81AH48963U | 50 mcg | 67% |
| Potassium UNII · RWP5GA015D | 49.5 mg | 1% |
| Boron Glycinate BoronUNII · YV58Q9ER5F | 1 mg | — |
| Vanadium UNII · 00J9J9XKDE | 100 mcg | — |
| Proprietary Mixed Carotenoid Blend Proprietary Blend (non-nutrient/non-botanical) | 425 mcg | — |
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 →
Other ingredients
Vegetarian Capsule · Ascorbyl Palmitate