supplementhackr
Universal Nutrition

Advanced Soy Pro Banana

Serving
33 Gram(s)
Per container
21
Form
powder
UPC
039442014382
DSLD
64005
Formula hash
a44f127e5812
Brand context
Universal Nutrition
Catalog
41
products
With avoid flag
1
products
FDA recalls
0
history
CAERS
4
reports
Caution-flaggedObjective label signals
Flagged excipients
2
0 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
1
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

14 active ingredients
IngredientAmount% DV
Calories
otherUNII · 1
125 Calorie(s)—
Total Fat
Fat (unspecified)other
1 Gram(s)2%
Total Carbohydrates
CarbohydrateotherUNII · 0
1 Gram(s)1%
Protein
Protein (unspecified)other
28 Gram(s)55%
Thiamine
ThiaminvitaminUNII · X66NSO3N35
3 effects
64 mcg4%
Riboflavin
vitaminUNII · TLM2976OFR
5 effects
32 mcg2%
Folate
vitaminUNII · 935E97BOY8
UL · set2 effects
64 mcg16%
Biotin
vitaminUNII · 6SO6U10H04
3 effects
10 mcg3%
Calcium
mineralUNII · SY7Q814VUP
UL · set6 effects
64 mg6%
Iron
mineralUNII · E1UOL152H7
UL · set5 effects
5 mg28%
Phosphorus
mineralUNII · 27YLU75U4W
UL · set2 effects
254 mg25%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
1.3 mg8%
Copper
mineralUNII · 789U1901C5
UL · set3 effects
445 mcg22%
Sodium
mineralUNII · 9NEZ333N27
287 mg12%
What this product supports · authorized claims

22 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
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 →

Other ingredients

isolated Soy Protein · Natural & Artificial flavors · Acesulfame Potassium

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.