Bronson

Lipacor

Serving

3 Capsule(s)

Form

capsule-unknown

UPC

716563884017

DSLD

8232

Formula hash

7d972164996b

Brand context

Bronson

Catalog

659

products

With avoid flag

products

FDA recalls

history

CAERS

reports

Avoid-flaggedObjective label signals

Flagged excipients

1 avoid · 1 caution

FDA recalls

no recall history

CAERS reports

FDA consumer events

Certifications

none recorded

1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

8 active ingredients

Ingredient	Amount	% DV
Vitamin E vitaminUNII · H4N855PNZ1 UL · set1 effect	10 IU	33%
Vitamin B3 Vitamin B3 (Niacin)vitamin	125 mg	625%
Chromium mineralUNII · 0R0008Q3JB 1 effect	34 mcg	28%
Policosanol herb	10 mg	—
Omega-3 Fish oil Fish OilotherUNII · XGF7L72M0F	166 mg	—
Plant Sterol Phytosterol (mixed)other	250 mg	—
Guggul Extract 10% Sterones GuggulherbUNII · 34969JX79R	33.3 mg	—
Garlic A-10,000 GarlicherbUNII · V1V998DC17	10 mg	—

What this product supports · authorized claims

2 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 macronutrient metabolism / normal blood glucose
from: Chromium
EFSAEU-Reg-432/2012-ID-260 →LOINC 2345-7
↓Protection from oxidative stress
from: Vitamin E
EFSAEU-Reg-432/2012-ID-160 →

Flagged excipients

2 flagged · authority citations

● AVOIDTitanium Dioxide
color
Banned in EU food products effective 2022-08 (Commission Regulation (EU) 2022/63) following EFSA Panel opinion that a safe daily intake could not be established due to genotoxicity concerns. Still GRAS in the US under 21 CFR 73.575 but EU position is stricter.
eur-lex.europa.eu →efsa.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

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

Gelatin · Microcrystalline Cellulose · Silica · Magnesium Stearate · Blue #1