Chaos and Pain

Cannibal Ferox

Serving
11 Gram(s)
Per container
25
Form
powder
DSLD
Recall historyObjective label signals
Flagged excipients
0
none
FDA recalls
3
3 Class I / II
CAERS reports
1
FDA consumer events
Certifications
0
none recorded
3 FDA recalls on file. · Every flag below links to the authority's published citation.

Supplement Facts

14 active ingredients
IngredientAmount% DV
Citrulline Malate
Citrulline malateUNII · PAB4036KHO
4000 mg
Creatine Monohydrate
CreatineUNII · 9603LN7R2Q
2000 mg
Betaine Anhydrous
UNII · 3SCV180C9W
1500 mg
N-Acetyl-L-Tyrosine
N-Acetyl TyrosineUNII · DA8G610ZO5
750 mg
Caffeine Anhydrous
CaffeineUNII · 3G6A5W338E
450 mg
Acacia rigidula
Blackbrush
200 mg
Higenamine
UNII · TBV5O16GAP
75 mg
Hordenine
UNII · K3489CA082
75 mg
Synephrine HCl
Synephrine
75 mg
Astragalus
UNII · N7J2VKV17X
25 mg
Panax notoginseng
San-Qi Ginseng
25 mg
Noopept
N-phenylacetyl-L-Prolylglycine ethyl esterUNII · 4QBJ98683M
20 mg
Bioperine
Black PepperUNII · KM66971LVF
10 mg
Yohimbine HCl
YohimbineUNII · 2Y49VWD90Q
3 mg
Recall history

3 FDA recalls

  1. Class II2016-11-08

    CANNIBAL FEROX AMPED, FACE-MELTING NOOTROPIC, PRE-WORKOUT ENERGY COMPLEX, STRAWBLOODY KIWI CRUSH, DIETARY SUPPLEMENT, NET. WT. 9.9 OZ (280g), Chaos and Pain, UPC 1056331460

    Reason: Product was analyzed and found to contain 1,3- dimethylbutylamine which was not declared on the label and is a prohibited substance.

    FDA record →
  2. 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 →
  3. 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 →

Other ingredients

Lemon Flavor · Acesulfame K · Sucralose · Maltodextrin · Sipernat