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Cellucor

C4 Ripped Tropical Punch

Serving
6 Gram(s)
Per container
30
Form
powder
UPC
842595100060
DSLD
82651
Formula hash
0bbfb75e22c7
Brand context
Cellucor
Catalog
476
products
With avoid flag
15
products
FDA recalls
0
history
CAERS
28
reports
Caution-flaggedObjective label signals
Flagged excipients
2
0 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
10
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

10 active ingredients
IngredientAmount% DV
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
250 mg417%
Niacin
vitaminUNII · 2679MF687A
UL · set3 effects
30 mg150%
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
500 mcg25%
Folate
vitaminUNII · 935E97BOY8
UL · set2 effects
250 mcg62%
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
35 mcg583%
Calcium
mineralUNII · SY7Q814VUP
UL · set6 effects
50 mg5%
Total Carbohydrates
CarbohydrateotherUNII · 0
1.6 Gram(s)—
Arginine alpha-ketoglutarate
Arginine Alpha Ketoglutarateherb
1 Gram(s)—
C4 Ripped Blend
Proprietary Blend (Combination)other
1 Gram(s)—
Explosive Energy Blend
Blend (Combination)other
371 mg—
What this product supports · authorized claims

14 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 Red #3
    color

    FDA revoked food/ingested-drug color additive approval for FD&C Red 3 in January 2025 (Docket FDA-2022-C-2886). Manufacturers have until January 2027 (foods) / January 2028 (ingested drugs) to reformulate.

    fda.gov →federalregister.gov →
FDA CAERS · adverse event context
10
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

Calcium Silicate · Silicon Dioxide · Natural Flavors · Malic Acid · Citric Acid · Sucralose · Acesulfame Potassium