Beachbody
SHAKEOLOGY <Greenberry/Chocolate>
LNHPD
6595056
Clean labelObjective label signals
Flagged excipients
0
none
FDA recalls
0
no recall history
CAERS reports
9
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
- GinkgoCategory D
LiverTox Category D (hepatotoxicity — separate concern from IARC Group 2B carcinogenicity classification). A handful of hepatitis reports.
LiverTox →
Supplement Facts
17 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Chlorella vulgaris | 350.0 mg | — |
| Lepidium meyenii Maca | 1000.0 mg | — |
| Ginkgo biloba GinkgoUNII · 19FUJ2C58T | 25.0 mg | — |
| Lactobacillus delbrueckii subsp. bulgaricus | 0.5 billion cfu | — |
| Vitis vinifera Grape | 50.0 mg | — |
| Copper UNII · 789U1901C5 | 800.0 mcg | — |
| Rosa canina Dog Rose | 50.0 mg | — |
| Pantothenic Acid Pantothenic Acid (Vitamin B5)UNII · 19F5HK2737 | 5.0 mg | — |
| Vitamin D UNII · 9VU1KI44GP | 5.0 mcg | — |
| Vitamin D UNII · 9VU1KI44GP | — | — |
| Bifidobacterium longum UNII · 831AQW699W | 0.5 billion cfu | — |
| Punica granatum Pomegranate | 250.0 mg | — |
| Iron UNII · E1UOL152H7 | 4.5 mg | — |
| Whey Protein Isolate ProteinUNII · 8617Z5FMF6 | 15000.0 mg | — |
| Smallanthus sonchifolius Yacon | 1000.0 mg | — |
| Vitamin C UNII · PQ6CK8PD0R | 180.0 mg | — |
| Euterpe oleracea | 150.0 mg | — |
What this product supports · authorized claims
13 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 D
- from: Vitamin D
- from: Copper · Iron · Vitamin C · Vitamin D
- from: Vitamin D
- from: Iron
- from: Iron
- from: Iron
- from: Vitamin C
- from: Vitamin C
- from: Copper
- from: Copper
- from: Iron · Vitamin C
- from: Vitamin C
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 →