Animal

Animal Cuts

Serving
1 Pack(s)
Per container
42
UPC
039442030146
DSLD
Formula hash
257f941d4d5a
Brand context
Catalog
139
products
With avoid flag
49
products
FDA recalls
0
history
CAERS
12
reports
Avoid-flaggedObjective label signals
Flagged excipients
5
1 avoid · 4 caution
FDA recalls
0
no recall history
CAERS reports
2
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · 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
800 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

5 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.

  • ◐ 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.

  • ◐ 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).

  • ◐ 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.

  • ◐ 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).

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 · Stearic Acid · Soy

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.