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Chaos and Pain

Cannibal Ferox Carny Candy

Serving
1 Scoop(s)
Per container
25
Form
powder
DSLD
209902
Formula hash
f91704332ab2
Brand context
Chaos and Pain
Catalog
9
products
With avoid flag
2
products
FDA recalls
3
history
CAERS
1
reports
Recall historyObjective label signals
Flagged excipients
0
none
FDA recalls
2
2 Class I / II
CAERS reports
1
FDA consumer events
Certifications
0
none recorded
2 FDA recalls on file. · Every flag below links to the authority's published citation.

Supplement Facts

13 active ingredients
IngredientAmount% DV
Citrulline Malate
Citrulline malateherbUNII · PAB4036KHO
4000 mg—
Beta-Alanine
amino_acidUNII · 11P2JDE17B
3200 mg—
Creatine Monohydrate
CreatineherbUNII · 9603LN7R2Q
2000 mg—
Betaine Anhydrous
herbUNII · 3SCV180C9W
1500 mg—
N-Acetyl-L-Tyrosine
N-Acetyl TyrosineherbUNII · DA8G610ZO5
500 mg—
Caffeine Anhydrous
CaffeineherbUNII · 3G6A5W338E
450 mg—
Orchilean
TBDherb
125 mg—
Isopropylnorsynephrine
herb
35 mg—
Halostachine
herb
40 mg—
Hordenine
herbUNII · K3489CA082
50 mg—
Yohimbine HCl
YohimbineherbUNII · 2Y49VWD90Q
2 mg—
Alpha Yohimbine
Rauwolscineherb
1.5 mg—
Huperzine-A
HuperzineherbUNII · 0111871I23
0.2 mg—
Recall history

2 FDA recalls

  1. Class II2016-08-10brand-level

    CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, UNICORN BLOOD, Chaos and Pain, DIETARY SUPPLEMENTS, NET.WT. 10.5 oz (300g), UPC 610563314669

    Reason: The products are being recalled because they contain 750 mg of Agmatine and 50 mg 1,3 Dimethylbutylamine per serving which is not declared on the label. 1,3 Dimethylbutylamine is not permitted for use in dietary supplements in the EU.

    FDA record →
  2. Class II2016-08-10brand-level

    CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, FIVE FINGER DEATH PUNCH, Chaos and Pain, DIETARY SUPPLEMENTS, NET.WT. 10.5 oz (300g), UPC 610563314652

    Reason: The products are being recalled because they contain 750 mg of Agmatine and 50 mg 1,3 Dimethylbutylamine per serving which is not declared on the label. 1,3 Dimethylbutylamine is not permitted for use in dietary supplements in the EU.

    FDA record →
FDA CAERS · adverse event context
1
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 →