supplementhackr
Chaos and Pain

Bacchus

Serving
3 Capsule(s)
Per container
30
Form
capsule-unknown
DSLD
209875
Formula hash
6aaa707e1a11
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

10 active ingredients
IngredientAmount% DV
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
25 mg1470%
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
200 mg220%
Sodium
mineralUNII · 9NEZ333N27
45 mg2%
Kanna
Sceletiumherb
1 Gram(s)—
Beta-Phenylethylamine
Phenethylamine (PEA)herb
250 mg—
Rhodiola rosea
Rhodiolaherb
200 mg—
Caffeine Anhydrous
CaffeineherbUNII · 3G6A5W338E
150 mg—
L-Theanine
TheanineherbUNII · 8021PR16QO
100 mg—
Hordenine HCl
Hordenineherb
100 mg—
5-HTP
amino_acidUNII · 9181P3OI6N
100 mg—
What this product supports · authorized claims

9 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.

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 →