Animal

Animal Stak

Serving
1 Pack(s)
Per container
21
UPC
039442030238
DSLD
Formula hash
7b90e8e2ef49
Brand context
Catalog
139
products
With avoid flag
49
products
FDA recalls
0
history
CAERS
12
reports
Avoid-flaggedObjective label signals
Flagged excipients
3
1 avoid · 2 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

9 active ingredients
IngredientAmount% DV
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
10.5 mg525%
Magnesium
mineralUNII · I38ZP9992A
6 effects
1.3× ULexceeds NIH ODS adult upper limitsource →
450 mg113%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
30 mg200%
Vitamin D3
Vitamin DvitaminUNII · 1C6V77QF41
UL · set4 effects
1000 IU250%
Pro Testosterone Complex
Blend (Herb/Botanical)other
1500 mg
Growth Hormone Support
Blend (Combination)other
1500 mg
Calories
otherUNII · 1
300 mg
Hormone Amplifying Blend
Blend (Combination)other
500 mg
Restorative Support Complex
Blend (Combination)other
500 mg
What this product supports · authorized claims

16 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.

Flagged excipients

3 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 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 · Magnesium Stearate · Silicon Dioxide · Stearic Acid · {FD&C Yellow} #6

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.