Beachbody
SHAKEOLOGY - Strawberry
LNHPD
20896980
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.
Supplement Facts
19 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Vitamin D UNII · 9VU1KI44GP | 5.0 micrograms | — |
| 4-alpha-D-Glucan glucanohydrolase | 171.0 FCC alpha-amylase dextrinizing units | — |
| Vitamin E UNII · H4N855PNZ1 | 12.46 mg AT | — |
| Vitamin E UNII · H4N855PNZ1 | 12.46 mg AT | — |
| Linum usitatissimum | 1800.0 milligrams | — |
| Dimethyl sulfone | 128.25 milligrams | — |
| Phosphorus UNII · 27YLU75U4W | 230.0 milligrams | — |
| Pea Protein Pea proteinUNII · 7Q50F46595 | 4405.0 milligrams | — |
| Smallanthus sonchifolius Yacon | 400.0 milligrams | — |
| Euterpe oleracea | 128.25 milligrams | — |
| Citrus Bioflavonoids Flavonoid (mixture)UNII · BD70459I50 | 42.75 milligrams | — |
| Vitamin B12 UNII · 8406EY2OQA | 6.0 micrograms | — |
| D-Pantothenic Acid Vitamin B5 (Pantothenic Acid) | 5.0 milligrams | — |
| Iodine UNII · 9679TC07X4 | 52.0 micrograms | — |
| Vitis vinifera Grape | 42.75 milligrams | — |
| alpha-D-Galactoside galactohydrolase | 12.8 FCC AGU | — |
| Whey Protein Isolate ProteinUNII · 8617Z5FMF6 | 13510.0 milligrams | — |
| Riboflavin UNII · TLM2976OFR | 1.3 milligrams | — |
| Camellia sinensis | 42.75 milligrams | — |
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: Phosphorus · Riboflavin · Vitamin B12
- from: Riboflavin
- from: Riboflavin
- from: Vitamin B12
- from: Vitamin D
- from: Phosphorus · Vitamin D
- from: Vitamin D
- from: Vitamin D
- from: Iodine
- from: Iodine
- from: Riboflavin · Vitamin E
- from: Riboflavin
- from: Vitamin B12
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 →