supplementhackr
Chaos and Pain

Red Sky

Serving
3 Capsule(s)
Per container
30
Form
tablet
DSLD
211418
Formula hash
12f454370f0b
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
Acetyl L-Carnitine
herbUNII · S3Z3R3X6RL
650 mg—
Caffeine Anhydrous
CaffeineherbUNII · 3G6A5W338E
300 mg—
Senegalia berlandieri extract
Acacia berlandieriherb
250 mg—
Green Coffee bean extract
Green CoffeeherbUNII · JFH385Y744
100 mg—
Thermo-V
Proprietary Blend (non-nutrient/non-botanical)other
100 mg—
Paradoxine
Grains of Paradiseherb
50 mg—
Higenamine
herbUNII · TBV5O16GAP
50 mg—
Hordenine
herbUNII · K3489CA082
50 mg—
Evodiamine
EvodiaherbUNII · C01825BVNL
25 mg—
Synephrine HCl
Synephrineherb
25 mg—
Bioperine
Black PepperherbUNII · KM66971LVF
10 mg—
Yohimbine HCl
YohimbineherbUNII · 2Y49VWD90Q
2 mg—
Alpha Yohimbine
Rauwolscineherb
1.5 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 →