Beachbody

SHAKEOLOGY Tropical Strawberry Vegan

LNHPD
21188232
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

23 active ingredients
IngredientAmount% DV
Withania somnifera
Ashwagandhaherb
LiverTox B
100.0 milligrams
1,4-alpha-D-Glucan glucohydrolase
other
3.0 FCC Glucoamylase Units
1,4-alpha-D-Glucan glucohydrolase
other
3.0 milligrams
Camellia sinensis
herb
48.0 milligrams
Salvia hispanica
other
2030.0 milligrams
Ginkgo biloba
GinkgoherbUNII · 19FUJ2C58T
LiverTox D
25.0 milligrams
Vaccinium corymbosum
other
239.0 milligrams
beta-D-fructofuranoside fructohydrolase
other
50.0 FCC Sumner units
beta-D-fructofuranoside fructohydrolase
other
0.5 milligrams
Myrciaria dubia
other
250.0 milligrams
Rice Protein
otherUNII · J9JP2XE45M
1360.0 milligrams
Fragaria chiloensis
other
985.0 milligrams
Dimethyl sulfone
other
150.0 milligrams
Moringa oleifera
Moringaherb
200.0 milligrams
Malpighia glabra
other
337.0 milligrams
4-alpha-D-Glucan glucanohydrolase
other
200.0 FCC alpha-amylase dextrinizing units
4-alpha-D-Glucan glucanohydrolase
other
5.0 milligrams
Inulin
otherUNII · JOS53KRJ01
51.0 milligrams
4-(1,3;1,4)-beta-D-Glucan 4-glucanohydrolase
other
300.0 FCC CU
4-(1,3;1,4)-beta-D-Glucan 4-glucanohydrolase
other
4.0 milligrams
Rose Hip
Rose (unspecified)herb
100.0 milligrams
Spinacia oleracea
other
150.0 milligrams
Chlorella vulgaris
other
475.0 milligrams
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 →