supplementhackr
Animal

Animal Cuts

Serving
2 Pack(s)
Per container
42
UPC
039442030146
DSLD
272884
Formula hash
b9733297dbc9
Brand context
Animal
Catalog
139
products
With avoid flag
49
products
FDA recalls
0
history
CAERS
12
reports
Caution-flaggedObjective label signals
Flagged excipients
4
0 avoid · 4 caution
FDA recalls
0
no recall history
CAERS reports
2
FDA consumer events
Certifications
0
none recorded
4 excipients carry authority-caution citations. · Every flag below links to the authority's published citation.

Supplement Facts

8 active ingredients
IngredientAmount% DV
Stimulant Complex
Blend (Combination)other
750 mg—
Metabolic Complex
Blend (Herb/Botanical)other
750 mg—
Thyroid Complex
Blend (Combination)other
350 mg—
Water Shedding Complex
Blend (Herb/Botanical)other
780 mg—
Nootropic Complex
Blend (Combination)other
500 mg—
Cortisol Inhibiting Complex
Blend (Combination)other
300 mg—
CCK Boosting Complex
Blend (Combination)other
300 mg—
Bioavailability Complex
Blend (Combination)other
500 mg—
Flagged excipients

4 flagged · authority citations

  • ◐ 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 →
  • ◐ CAUTIONFD&C Blue #1
    color

    EU requires 'attention in children' warning per Commission Regulation 1333/2008 Annex III. Limited to specific food categories; capsule-shell use permitted with restrictions.

    eur-lex.europa.eu →
  • ◐ CAUTIONFD&C Yellow #5
    color

    EU requires warning label 'may have an adverse effect on activity and attention in children' per Commission Regulation 1333/2008 Annex III (following Southampton study 2007). FDA requires specific label declaration (21 CFR 74.705).

    eur-lex.europa.eu →ecfr.gov →
  • ◐ CAUTIONFD&C Yellow #6
    color

    EU requires 'attention in children' warning per Reg 1333/2008 Annex III (Southampton study 2007). Banned in Norway + Finland; allowed in US under 21 CFR 74.706 with declaration.

    eur-lex.europa.eu →
FDA CAERS · adverse event context
2
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

Gelatin · Dicalcium Phosphate · DMAE Bitartrate · Microcrystalline Cellulose · Magnesium Stearate · Silicon Dioxide · Stearic Acid