Beachbody

Shakeology <Greenberry/Chocolate>

LNHPD
6903780
Formula hash
973632d727b6
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

19 active ingredients
IngredientAmount% DV
Chromium
mineralUNII · 0R0008Q3JB
1 effect
60.0 mcg
Molybdenum
mineralUNII · 81AH48963U
UL · set1 effect
30.0 mcg
Schisandra chinensis
SchisandraherbUNII · RM13YIU944
50.0 mg
Iodine
mineralUNII · 9679TC07X4
UL · set2 effects
52.2 mcg
Ganoderma lucidum
Reishi mushroomotherUNII · J5P04QW0CF
100.0 mg
Methylsulfonylmethane
herbUNII · 9H4PO4Z4FT
150.0 mg
Lepidium meyenii
Macaherb
1000.0 mg
Magnesium
mineralUNII · I38ZP9992A
UL · set6 effects
80.0 mg
Vitis vinifera
Grapeherb
50.0 mg
Ophiocordyceps sinensis
other
100.0 mg
Linum usitatissimum
other
700.0 mg
Lactobacillus casei
otherUNII · SA940P2U00
0.5 billion cfu
Lactobacillus acidophilus
otherUNII · 1PRR1V42V5
1.25 billion cfu
Biotin
vitaminUNII · 6SO6U10H04
3 effects
90.0 mcg
Ginkgo biloba
GinkgoherbUNII · 19FUJ2C58T
LiverTox D
25.0 mg
Chlorella vulgaris
other
350.0 mg
Spirulina platensis
Blue-Green Algaeother
350.0 mg
Lactobacillus acidophilus
otherUNII · 1PRR1V42V5
0.5 billion cfu
Calcium
mineralUNII · SY7Q814VUP
UL · set6 effects
500.0 mg
What this product supports · authorized claims

14 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 →