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Animal

Animal Rage XL Mango Unchained

Serving
4 Gram(s)
Per container
30
Form
powder
UPC
039442031037
DSLD
37849
Formula hash
a02a4f1ef92b
Brand context
Animal
Catalog
139
products
With avoid flag
49
products
FDA recalls
0
history
CAERS
12
reports
Caution-flaggedObjective label signals
Flagged excipients
2
0 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
2
FDA consumer events
Certifications
0
none recorded
2 excipients carry authority-caution citations. · Every flag below links to the authority's published citation.

Supplement Facts

12 active ingredients
IngredientAmount% DV
Niacin
vitaminUNII · 2679MF687A
UL · set3 effects
15 mg75%
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
5 mcg83%
Calcium
mineralUNII · SY7Q814VUP
UL · set6 effects
5 mg1%
Magnesium
mineralUNII · I38ZP9992A
UL · set6 effects
2.5 mg1%
Chloride
mineralUNII · Q32ZN48698
15 mg1%
Sodium
mineralUNII · 9NEZ333N27
10 mg1%
Potassium
mineralUNII · RWP5GA015D
3 effects
14 mg1%
Calories
otherUNII · 1
3635 mg—
Endurance & Perfomance Complex
Blend (Combination)other
0 NP—
Focus & Intensity Complex
Blend (Combination)other
0 NP—
Sustained Energy Complex
Blend (Combination)other
0 NP—
Quick Energy Complex
Blend (Combination)other
0 NP—
What this product supports · authorized claims

12 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

2 flagged · authority citations

  • ◐ 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

Natural & Artificial flavors · Citric Acid · Malic Acid · Acesulfame Potassium · Sucralose · Potassium Chelate

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.