supplementhackr
BSN

N.O.-Xplode 2.0 Orange

Serving
22 Gram(s)
Per container
50
Form
powder
UPC
834266009343
DSLD
18897
Formula hash
e4f1b04ddbac
Brand context
BSN
Catalog
224
products
With avoid flag
9
products
FDA recalls
0
history
CAERS
6
reports
Caution-flaggedObjective label signals
Flagged excipients
2
0 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
6
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

11 active ingredients
IngredientAmount% DV
Calories
otherUNII · 1
25 {Calories}—
Total Carbohydrates
CarbohydrateotherUNII · 0
6 g2%
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
20 mg1000%
Folate
vitaminUNII · 935E97BOY8
UL · set2 effects
300 mcg75%
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
120 mcg2000%
Calcium
mineralUNII · SY7Q814VUP
UL · set6 effects
75 mg8%
Phosphorus
mineralUNII · 27YLU75U4W
UL · set2 effects
200 mg20%
Magnesium
mineralUNII · I38ZP9992A
UL · set6 effects
60 mg15%
Sodium
mineralUNII · 9NEZ333N27
300 mg13%
Potassium
mineralUNII · RWP5GA015D
3 effects
75 mg2%
N.O.-Xplode's Proprietary Blend
Proprietary Blend (Combination)other
19.6 g—
What this product supports · authorized claims

13 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 #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 →
  • ◐ 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 →
FDA CAERS · adverse event context
6
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

Citric Acid · Natural & Artificial flavors · Potassium Citrate · Sucralose · Calcium Silicate · Acesulfame Potassium