Nature's Plus
Ultra Virile-Actin
Brand context
Catalog
1,639
products
With avoid flag
0
products
FDA recalls
0
history
CAERS
23
reports
Clean labelObjective label signals
Flagged excipients
0
none
FDA recalls
0
no recall history
CAERS reports
21
FDA consumer events
Certifications
0
none recorded
No authority-flagged excipients or recalls. · Every flag below links to the authority's published citation.
NIH LiverTox
1 ingredient with hepatotoxicity classification
Worst severity: Category D
- Saw PalmettoCategory D
LiverTox Category D. Rare cases of acute hepatitis reported; causality uncertain. Some reports confounded by concurrent pharmaceuticals.
LiverTox →
Supplement Facts
16 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Vitamin E vitaminUNII · H4N855PNZ1 UL · set1 effect | 200 IU | 667% |
| Vitamin B6 vitaminUNII · KV2JZ1BI6Z UL · set6 effects | 5 mg | 250% |
| Olive Leaf Extract OliveherbUNII · MJ95C3OH47 | 50 mg | 333% |
| Rhodiola herbUNII · 11R149C3CY | 100 mg | — |
| Eleuthero Eleuthero RootherbUNII · ZQH6VH092Z | 100 mg | — |
| Bee Pollen otherUNII · 3729L8MA2C | 75 mg | — |
| Saw Palmetto herbUNII · J7WWH9M8QS LiverTox D | 60 mg | — |
| Brazilian Muira Puama Muira Puamaherb | 50 mg | — |
| L-Histidine Histidineamino_acidUNII · 4QD397987E | 50 mg | — |
| Cayenne Capsicumherb | 50 mg | — |
| L-Phenylalanine Phenylalanineamino_acidUNII · 47E5O17Y3R | 50 mg | — |
| St. John's Wort herbUNII · A6V4CUE7PV LiverTox D | 50 mg | — |
| Royal Jelly otherUNII · L497I37F0C | 25 mg | — |
| L-Carnitine herbUNII · 0G389FZZ9M | 25 mg | — |
| Pacific Oyster extract OysterotherUNII · FX2S0D3781 | 10 mg | — |
| Coenzyme Q10 herb | 2500 mcg | — |
What this product supports · authorized claims
7 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: Vitamin B6
- from: Vitamin B6
- from: Vitamin E
- from: Vitamin B6
- from: Vitamin B6
FDA CAERS · adverse event context
21
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
Di-Calcium Phosphate · Microcrystalline Cellulose · Stearic Acid · Magnesium Stearate · Silica · Vegetable Cellulose · Pharmaceutical Glaze
Chemically equivalent
Same formula, different brand
Products with identical sorted (ingredient, amount) tuples.