Mason Natural

Ferrous Gluconate

Serving

1 Tablet(s)

Form

tablet

UPC

311845137517

DSLD

214470

Formula hash

dd9a0b5fcf63

Brand context

Mason Natural

Catalog

249

products

With avoid flag

products

FDA recalls

history

CAERS

reports

Avoid-flaggedObjective label signals

Flagged excipients

1 avoid · 2 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

1 active ingredients

Ingredient	Amount	% DV
Iron mineralUNII · E1UOL152H7 UL · set5 effects	27 mg	150%

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 formation of red blood cells + hemoglobin
from: Iron
EFSAEU-Reg-432/2012-ID-249 →LOINC 789-8
↑Normal cognitive function
from: Iron
EFSAEU-Reg-432/2012-ID-253 →
↑Normal oxygen transport in the body
from: Iron
EFSAEU-Reg-432/2012-ID-252 →LOINC 718-7
↑Normal immune system function
from: Iron
EFSAEU-Reg-432/2012-ID-254 →
↓Reduction of tiredness and fatigue
from: Iron
EFSAEU-Reg-432/2012-ID-255 →

Flagged excipients

3 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 Blue #1 Lake
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 #6 Lake
color
EU requires 'attention in children' warning per Reg 1333/2008 Annex III (Southampton study 2007). Banned in Norway + Finland; allowed in US under 21 CFR 74.706 with declaration.
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

Microcrystalline Cellulose · Croscarmellose Sodium · Stearic Acid · Hypromellose · Magnesium Silicate · Triacetin · Mineral Oil · Riboflavin

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.