Chaos and Pain

Chemical Four

Serving

1 Tablet(s)

Per container

Form

tablet

DSLD

267070

Formula hash

c15e8e67388c

Brand context

Chaos and Pain

Catalog

products

With avoid flag

products

FDA recalls

history

CAERS

reports

Avoid-flaggedObjective label signals

Flagged excipients

1 avoid · 1 caution

FDA recalls

2 Class I / II

CAERS reports

FDA consumer events

Certifications

none recorded

1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

4 active ingredients

Ingredient	Amount	% DV
4-DHEA Blend 4-androsteroneherb	75 mg	—
Total Carbohydrates CarbohydrateotherUNII · 0	150 mg	—
Epicatechin epicatechinherbUNII · 34PHS7TU43	150 mg	—
6,7-Dihydroxybergamottin herb	50 mg	—

Flagged excipients

2 flagged · authority citations

● AVOIDTitanium Dioxide
color
Banned in EU food products effective 2022-08 (Commission Regulation (EU) 2022/63) following EFSA Panel opinion that a safe daily intake could not be established due to genotoxicity concerns. Still GRAS in the US under 21 CFR 73.575 but EU position is stricter.
eur-lex.europa.eu →efsa.europa.eu →ecfr.gov →
◐ CAUTIONFD&C Red #40
color
EU requires the same 'attention/activity in children' warning label as Yellow 5 per Commission Regulation 1333/2008 Annex III. California enacted a public-school ban effective 2028 (AB 2316, 2024).
eur-lex.europa.eu →leginfo.legislature.ca.gov →

Recall history

2 FDA recalls

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 →
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

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

Microcrystalline · Phosphatidylcholine · Hydroxypropyl-Beta-Cyclodextrin · Phytosterol · Stearic Acid · Magnesium Stearate · Starch · Silica