Fragrance avoidance
No fragrance-linked caution surfaced in the current profile.
This ingredient does not currently read as a fragrance-linked driver in the published evidence and hazard profile.
YELLOWFIN TUNA
FDA NDC lists this ingredient in 2 active drug products and 2 total products.
Research docs0Claims0Sources4FunctionFunction pendingIdentifierdrug bank:DB15541
Concern score
5/100Low concern based on regulatory listings.
Well researched
How we scored this
The concern value reflects this ingredient's chemical identity — its hazard profile from the published classifications and regulatory status below — not the safety of a product it appears in. A score near 40 is the baseline for ingredients with no specific signal (water scores 40 by design), so a mid-range value is not a safety verdict.
Concern score 5/100 (low) · high confidence.
Where it appears
Prevalence of YELLOWFIN TUNA in our catalog (fda_ndc).
Products
2
Catalog
Found in these products
Co-occurrence
Often appears with
Ingredients that frequently appear alongside YELLOWFIN TUNA in the catalog.
Suitability
Context-specific fit derived from published classifications and the current ingredient evidence profile.
Good fit
Evidence read
The published evidence profile currently shaping this ingredient record.
No evidence profiles are attached to this ingredient yet.
Allergen profile
Canonical allergen markers detected on this ingredient. Each row is derived from the ingredient’s name or synonyms matching a known allergen class — useful when scanning a label for a specific allergy context.
- FishContains · Oral (ingested)
Source: chemindex_name_match
- ShellfishContains · Oral (ingested)
Source: chemindex_name_match
Linked research
Primary documents currently linked to this ingredient record.
No linked research documents are attached to this ingredient yet.
Extracted claims
Structured claim signals pulled from linked ingredient research.
No extracted claims are attached to this ingredient yet.
Regulatory status
Published jurisdiction-level classifications and regulatory designations for this ingredient.
US
FDA
FDA NDC lists this ingredient in 2 active drug products and 2 total products.
Effective: 2026-12-31View source →
US
FDA
openFDA substance registry classifies this ingredient as structurallydiverse.
Effective: 2026-05-24View source →
US
FDA
openFDA substance registry classifies this ingredient as concept.
