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GNC Beyond Raw

LIT AF Gummy Worm

Serving
22 Gram(s)
Per container
20
Form
powder
UPC
048107096960
DSLD
335662
Formula hash
af3763b5c62b
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

14 active ingredients
IngredientAmount% DV
Calories
otherUNII · 1
20 Calorie(s)—
Total Carbohydrates
CarbohydrateotherUNII · 0
5 Gram(s)2%
Calcium
mineralUNII · SY7Q814VUP
UL · set6 effects
150 mg12%
Sodium
mineralUNII · 9NEZ333N27
40 mg2%
Potassium
mineralUNII · RWP5GA015D
3 effects
200 mg4%
L-Citrulline Malate
Citrulline malateherbUNII · PAB4036KHO
8 Gram(s)—
Beta-Alanine
amino_acidUNII · 11P2JDE17B
3.2 Gram(s)—
BetaPower
Betaine Anhydrousherb
2.5 Gram(s)—
Creatine
herbUNII · MU72812GK0
2 Gram(s)—
Total Carbohydrates
CarbohydrateotherUNII · 0
1.5 Gram(s)—
Taurine
herbUNII · 1EQV5MLY3D
1 Gram(s)—
Peak ATP
Adenosine triphosphateherb
400 mg—
Caffeine Blend
Blend (Herb/Botanical)other
300 mg—
Alpha Glycerophosphocholine
Alpha-GPCherb
150 mg—
What this product supports · authorized claims

8 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 Blue #1
    color

    EU requires 'attention in children' warning per Commission Regulation 1333/2008 Annex III. Limited to specific food categories; capsule-shell use permitted with restrictions.

    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
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 · Acesulfame Potassium · acetylated Monoglycerides · Calcium Carbonate · Calcium Silicate · Dicalcium Phosphate · Glycerin · Polysorbate 80 · Potassium Citrate · Potassium Sorbate · Shellac · Silicon Dioxide · Sucralose · Talc