Beachbody
SHAKEOLOGY Strawberry with Bacillus coagulans
LNHPD
21198606
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
18 active ingredients| Ingredient | Amount | % DV |
|---|---|---|
| Withania somnifera Ashwagandha | 86.0 milligrams | — |
| Mixed tocopherol concentrate Vitamin E (mixed tocopherols)UNII · R0ZB2556P8 | 35.0 milligrams | — |
| Astragalus membranaceus AstragalusUNII · 922OP8YUPF | 227.0 milligrams | — |
| Zinc UNII · J41CSQ7QDS | 6.0 milligrams | — |
| Vitamin B6 UNII · KV2JZ1BI6Z | 2.0 milligrams | — |
| Cinnamomum aromaticum Cinnamon | 42.0 milligrams | — |
| Chenopodium quinoa | 10.0 milligrams | — |
| Linum usitatissimum | 1800.0 milligrams | — |
| Moringa oleifera Moringa | 21.0 milligrams | — |
| Rose Hip Rose (unspecified) | 129.0 milligrams | — |
| Brassica oleracea var. viridis | 86.0 milligrams | — |
| Spinacia oleracea | 171.0 milligrams | — |
| 4-alpha-D-Glucan glucanohydrolase | 172.0 FCC alpha-amylase dextrinizing units | — |
| 4-alpha-D-Glucan glucanohydrolase | 4.3 milligrams | — |
| Folate UNII · 935E97BOY8 | 200.0 micrograms | — |
| Ganoderma lucidum Reishi mushroomUNII · J5P04QW0CF | 137.0 milligrams | — |
| 4-(1,3;1,4)-beta-D-Glucan 4-glucanohydrolase | 258.0 FCC CU | — |
| 4-(1,3;1,4)-beta-D-Glucan 4-glucanohydrolase | 3.44 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: Vitamin B6
- from: Vitamin B6
- from: Vitamin B6 · Zinc
- from: Folate · Vitamin B6
- from: Zinc
- from: Zinc
- from: Zinc
- from: Zinc
- from: Zinc
- from: Zinc
- from: Folate · Vitamin B6
- from: Vitamin B6
- from: Zinc
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 →