GNC Multivitamin
Solotron
Clean labelObjective label signals
Flagged excipients
0
none
FDA recalls
0
no recall history
CAERS reports
11
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
34 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Vitamin A UNII · 81G40H8B0T | 10000 IU | 200% |
| Vitamin C UNII · PQ6CK8PD0R | 200 mg | 333% |
| Vitamin D2 Vitamin DUNII · VS041H42XC | 400 IU | 100% |
| Vitamin E UNII · H4N855PNZ1 | 30 IU | 100% |
| Vitamin K UNII · A034SE7857 | 25 mcg | 31% |
| Thiamine ThiaminUNII · X66NSO3N35 | 30 mg | 2000% |
| Riboflavin UNII · TLM2976OFR | 30 mg | 1765% |
| Niacin UNII · 2679MF687A | 30 mg | 150% |
| Vitamin B6 UNII · KV2JZ1BI6Z | 30 mg | 1500% |
| Folate UNII · 935E97BOY8 | 400 mcg | 100% |
| Vitamin B12 UNII · 8406EY2OQA | 30 mcg | 500% |
| Biotin UNII · 6SO6U10H04 | 30 mcg | 10% |
| Pantothenic Acid Pantothenic Acid (Vitamin B5)UNII · 19F5HK2737 | 30 mg | 300% |
| Calcium UNII · SY7Q814VUP | 60 mg | 6% |
| Iron UNII · E1UOL152H7 | 18 mg | 100% |
| Iodine UNII · 9679TC07X4 | 150 mcg | 100% |
| Magnesium UNII · I38ZP9992A | 30 mg | 8% |
| Zinc UNII · J41CSQ7QDS | 30 mg | 200% |
| Selenium UNII · H6241UJ22B | 25 mcg | 36% |
| Copper UNII · 789U1901C5 | 500 mcg | 25000% |
| Manganese UNII · 42Z2K6ZL8P | 5 mg | 250% |
| Chromium UNII · 0R0008Q3JB | 25 mcg | 21% |
| Molybdenum UNII · 81AH48963U | 25 mcg | 33% |
| Potassium UNII · RWP5GA015D | 30 mg | 1% |
| Choline UNII · N91BDP6H0X | 14 mg | — |
| Para-Aminobenzoic Acid PABAUNII · TL2TJE8QTX | 30 mg | — |
| Citrus Bioflavonoids Complex Flavonoid (mixture) | 25 mg | — |
| Green Tea leaves extract Green Tea | 5 mg | — |
| N-Acetyl L-Cysteine N-Acetyl CysteineUNII · WYQ7N0BPYC | 500 mcg | — |
| Lutein UNII · X72A60C9MT | 300 mcg | — |
| Boron UNII · N9E3X5056Q | 100 mcg | — |
| Inositol UNII · 4L6452S749 | 30 mcg | — |
| Vanadium UNII · 00J9J9XKDE | 10 mcg | — |
| Silicon UNII · Z4152N8IUI | 10 mcg | — |
FDA CAERS · adverse event context
11
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 →