Stacker 2

Xtra Energy Shot Grape Flavor

Serving

1 Bottle(s)

Form

liquid

DSLD

33432

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 UNII · 1	0 {Calories}	—
Niacin UNII · 2679MF687A	20 mg	100%
Vitamin B6 UNII · KV2JZ1BI6Z	40 mg	200%
Folate UNII · 935E97BOY8	400 mcg	100%
Vitamin B12 UNII · 8406EY2OQA	500 Nordic Berry(ies)	8333%
Sodium UNII · 9NEZ333N27	10 mg	1%
Proprietary Energy Blend Proprietary Blend (Combination)	2125 mg	—
Enzyme Blend Blend (non-nutrient/non-botanical)	1 mg	—

What this product supports · authorized claims

6 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 · Vitamin B12 · Vitamin B6
EFSAEU-Reg-432/2012-ID-43 →
↑Normal nervous system function
from: Niacin · Vitamin B6
EFSAEU-Reg-432/2012-ID-44 →
↑Normal immune system function
from: Vitamin B6
EFSAEU-Reg-432/2012-ID-73 →
↑Normal formation of red blood cells + hemoglobin
from: Folate · Vitamin B12 · Vitamin B6
EFSAEU-Reg-432/2012-ID-67 →LOINC 789-8
↓Reduction of tiredness and fatigue
from: Niacin · Vitamin B6
EFSAEU-Reg-432/2012-ID-47 →
↓Normal homocysteine metabolism
from: Folate · Vitamin B12 · Vitamin B6
EFSAEU-Reg-432/2012-ID-77 →LOINC 13965-9

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

filtered Water · Natural and Artificial flavors · Potassium Sorbate · SODIUM BENZOATE · Sucralose