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GNC Beyond Raw

Ravage Orange

Serving
26 Gram(s)
Per container
20
Form
powder
UPC
048107107123
DSLD
12800
Formula hash
07c45cf652fd
Brand context
GNC Beyond Raw
Catalog
212
products
With avoid flag
33
products
FDA recalls
0
history
CAERS
9
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
Calories
otherUNII · 1
15 {Calories}—
Total Fat
Fat (unspecified)other
0.5 g1%
Total Carbohydrates
CarbohydrateotherUNII · 0
2 g1%
Niacin
vitaminUNII · 2679MF687A
UL · set3 effects
30 mg150%
Calcium
mineralUNII · SY7Q814VUP
UL · set6 effects
40 mg4%
Chloride
mineralUNII · Q32ZN48698
190 mg6%
Sodium
mineralUNII · 9NEZ333N27
80 mg3%
Potassium
mineralUNII · RWP5GA015D
3 effects
140 mg4%
Anabolic Muscle Primer
Blend (Combination)other
5.3 g—
Muscle Buffering System
Blend (Combination)other
3.2 g—
N.O. Vasodilation Amplifier
Blend (Combination)other
3.1 g—
Thermo Energy Intensifier
Blend (Combination)other
603.3 mg—
What this product supports · authorized claims

9 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 #40
    color

    EU requires the same 'attention/activity in children' warning label as Yellow 5 per Commission Regulation 1333/2008 Annex III. California enacted a public-school ban effective 2028 (AB 2316, 2024).

    eur-lex.europa.eu →leginfo.legislature.ca.gov →
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 and Artificial flavors · Citric Acid · Malic Acid · Lecithin · Calcium Silicate · Silicon Dioxide · Sucralose · Acesulfame Potassium