GNC GenetixHD

Hyper-Charge Grape

Serving

10 Gram(s)

Per container

Form

powder

UPC

048107154004

DSLD

42266

Formula hash

25c3362c1530

Brand context

GNC GenetixHD

Catalog

products

With avoid flag

products

FDA recalls

history

CAERS

reports

Caution-flaggedObjective label signals

Flagged excipients

0 avoid · 2 caution

FDA recalls

no recall history

CAERS reports

FDA consumer events

Certifications

none recorded

2 excipients carry authority-caution citations. · Every flag below links to the authority's published citation.

Supplement Facts

8 active ingredients

Ingredient	Amount	% DV
Calories otherUNII · 1	15 {Calories}	—
Total Carbohydrates CarbohydrateotherUNII · 0	2.5 Gram(s)	1%
Niacin vitaminUNII · 2679MF687A UL · set3 effects	20 mg	100%
Sodium mineralUNII · 9NEZ333N27	25 mg	1%
Potassium mineralUNII · RWP5GA015D 3 effects	20 mg	1%
Elite Pump Factor Blend (Combination)other	0 NP	—
Hyper-Thermogenic Trigger Blend (Combination)other	0 NP	—
Neuro-Charger Matrix Blend (Combination)other	0 NP	—

What this product supports · authorized claims

5 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.

↑Normal energy-yielding metabolism
from: Niacin
EFSAEU-Reg-432/2012-ID-43 →
↑Normal nervous system function
from: Niacin · Potassium
EFSAEU-Reg-432/2012-ID-44 →
↑Normal muscle function
from: Potassium
EFSAEU-Reg-432/2012-ID-320 →
↓Reduction of tiredness and fatigue
from: Niacin
EFSAEU-Reg-432/2012-ID-47 →
↓Maintenance of normal blood pressure
from: Potassium
EFSAEU-Reg-432/2012-ID-323 →LOINC 8480-6

Flagged excipients

2 flagged · authority citations

◐ 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 →
◐ 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 →

FDA CAERS · adverse event context

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

Gum Arabic · Citric Acid · Natural and Artificial flavors · Tartaric Acid · Silica · Sucralose · Maltodextrin · Acesulfame Potassium

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.