Pharmanex
LifePak Women
Serving
1 Packet(s)
DSLD
Avoid-flaggedObjective label signals
Flagged excipients
1
1 avoid · 0 caution
FDA recalls
0
no recall history
CAERS reports
2
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.
Supplement Facts
31 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Vitamin A UNII · 81G40H8B0T | 2250 mcg RAE | 250% |
| Vitamin C UNII · PQ6CK8PD0R | 250 mg | 278% |
| Vitamin D UNII · 9VU1KI44GP | 5 mcg | 25% |
| Vitamin E UNII · H4N855PNZ1 | 101 mg | 673% |
| Vitamin K UNII · A034SE7857 | 20 mcg | 17% |
| Thiamine ThiaminUNII · X66NSO3N35 | 3.75 mg | 313% |
| Riboflavin UNII · TLM2976OFR | 4.25 mg | 327% |
| Niacin UNII · 2679MF687A | 20 mg NE | 125% |
| Vitamin B6 UNII · KV2JZ1BI6Z | 50 mg | 2941% |
| Folate UNII · 935E97BOY8 | 500 mcg DFE | 125% |
| Vitamin B12 UNII · 8406EY2OQA | 15 mcg | 625% |
| Biotin UNII · 6SO6U10H04 | 150 mcg | 500% |
| Pantothenic Acid Pantothenic Acid (Vitamin B5)UNII · 19F5HK2737 | 15 mg | 300% |
| Calcium UNII · SY7Q814VUP | 500 mg | 38% |
| Phosphorus UNII · 27YLU75U4W | 100 mg | 8% |
| Iron UNII · E1UOL152H7 | 5 mg | 28% |
| Iodine UNII · 9679TC07X4 | 50 mcg | 33% |
| Magnesium UNII · I38ZP9992A | 250 mg | 60% |
| Zinc UNII · J41CSQ7QDS | 7.5 mg | 68% |
| Selenium UNII · H6241UJ22B | 70 mcg | 127% |
| Copper UNII · 789U1901C5 | 0.5 mg | 56% |
| Manganese UNII · 42Z2K6ZL8P | 1 mg | 43% |
| Chromium UNII · 0R0008Q3JB | 100 mcg | 286% |
| Molybdenum UNII · 81AH48963U | 37.5 mcg | 83% |
| Cranberry powder cranberryUNII · 0MVO31Q3QS | 125 mg | — |
| Inositol UNII · 4L6452S749 | 125 mg | — |
| Polyphenol and Flavonoid Blend Blend (non-nutrient/non-botanical) | 62.5 mg | — |
| Alpha Lipoic Acid UNII · 73Y7P0K73Y | 25 mg | — |
| Carotenoid Blend Carotenoid | 3.5 mg | — |
| Boron UNII · N9E3X5056Q | 1.5 mg | — |
| Vanadium UNII · 00J9J9XKDE | 10 mcg | — |
Flagged excipients
1 flagged · authority citations
- ● AVOIDTitanium Dioxidecolor
Banned in EU food products effective 2022-08 (Commission Regulation (EU) 2022/63) following EFSA Panel opinion that a safe daily intake could not be established due to genotoxicity concerns. Still GRAS in the US under 21 CFR 73.575 but EU position is stricter.
FDA CAERS · adverse event context
2
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
Gelatin · Microcrystalline Cellulose · Croscarmellose Sodium · Stearic Acid · Magnesium Stearate · Silicon Dioxide