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Avoid-flaggedObjective label signals

Flagged excipients

4

1 avoid · 3 caution

FDA recalls

0

no recall history

CAERS reports

2

FDA consumer events

Certifications

0

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

4 flagged · authority citations

● AVOIDTitanium Dioxide
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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 #2 Carmine
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Banned from direct food use in Norway; restricted in EU under Commission Regulation 1333/2008. FDA permits under 21 CFR 74.102 with labeling requirement.
eur-lex.europa.eu →
◐ CAUTIONFD&C Red #40
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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 Yellow #5
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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

Dextrose · Cellulose · Croscarmellose Sodium · Stearic Acid · Magnesium Silicate · Magnesium Stearate · PEG · Silicon Dioxide

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.