Beachbody

SHAKEOLOGY Greenberry with Bacillus Coagulans

LNHPD
21189012
Brand context
CA
Catalog
62
products
With avoid flag
0
products
FDA recalls
0
history
CAERS
17
reports
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
About LiverTox →
  • GinkgoCategory D

    LiverTox Category D (hepatotoxicity — separate concern from IARC Group 2B carcinogenicity classification). A handful of hepatitis reports.

    LiverTox →

Supplement Facts

16 active ingredients
IngredientAmount% DV
Malpighia glabra
other
294.0 milligrams
Niacinamide
NiacinvitaminUNII · 25X51I8RD4
UL · set3 effects
5.0 milligrams
Biotin
vitaminUNII · 6SO6U10H04
3 effects
90.0 micrograms
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
2.0 milligrams
Beta-Carotene
Vitamin AvitaminUNII · 01YAE03M7J
UL · set3 effects
3000.0 micrograms
Phosphorus
mineralUNII · 27YLU75U4W
UL · set2 effects
230.0 milligrams
Myrciaria dubia
other
310.0 milligrams
Smallanthus sonchifolius
Yaconherb
400.0 milligrams
Astragalus membranaceus
AstragalusherbUNII · 922OP8YUPF
227.0 milligrams
Folate
vitaminUNII · 935E97BOY8
UL · set2 effects
200.0 micrograms
Ginkgo biloba
GinkgoherbUNII · 19FUJ2C58T
LiverTox D
21.0 milligrams
4-(1,3;1,4)-beta-D-Glucan 4-glucanohydrolase
other
258.0 FCC CU
4-(1,3;1,4)-beta-D-Glucan 4-glucanohydrolase
other
3.44 milligrams
Salvia hispanica
other
1050.0 milligrams
Lepidium meyenii
Macaherb
55.0 milligrams
Lycium Barbarum
GojiherbUNII · 766SVR5GCU
171.0 milligrams
What this product supports · authorized claims

10 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.

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 →