Irwin Naturals

Ginkgo Smart

Serving
2 Liquid Softgel(s)
Per container
60
Form
capsule-unknown
UPC
710363578268
DSLD
Formula hash
725ece544634
Brand context
Catalog
314
products
With avoid flag
269
products
FDA recalls
0
history
CAERS
12
reports
Avoid-flaggedObjective label signals
Flagged excipients
1
1 avoid · 0 caution
FDA recalls
0
no recall history
CAERS reports
11
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.
NIH LiverTox
1 ingredient with hepatotoxicity classification
Worst severity: Category D
About LiverTox →
  • GinkgoCategory D

    LiverTox Category D (hepatotoxicity — separate concern from IARC Group 2B carcinogenicity classification). A handful of hepatitis reports.

    LiverTox →

Supplement Facts

15 active ingredients
IngredientAmount% DV
Calories
otherUNII · 1
15 Calorie(s)
Total Fat
Fat (unspecified)other
1 Gram(s)1%
Cholesterol
otherUNII · 97C5T2UQ7J
5 mg1%
Protein
Protein (unspecified)other
1 Gram(s)
Choline
vitaminUNII · N91BDP6H0X
UL · set3 effects
30 mg5%
Fish Oil
otherUNII · XGF7L72M0F
600 mg
Ginkgo powder
Ginkgoherb
LiverTox D
400 mg
Ginkgo biloba
GinkgoherbUNII · 19FUJ2C58T
LiverTox D
120 mg
Dimethylaminoethanol Bitartrate
DeanolherbUNII · D240J05W14
40 mg
Trimethylglycerine Hydrochloride
Betaineherb
25 mg
Acetyl L-Carnitine
herbUNII · S3Z3R3X6RL
40 mg
Alpha Lipoic Acid
herbUNII · 73Y7P0K73Y
15 mg
Velvet Bean Seed Extract
Cowhageherb
10 mg
Toothed Clubmoss extract
Chinese Club Mossherb
1 mg
BioPerine Complex
Proprietary Blendother
6 mg
What this product supports · authorized claims

3 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.

Flagged excipients

1 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.

FDA CAERS · adverse event context
11
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 · Water, Purified · Glycerin · Soy Lecithin · Beeswax · Turmeric · Maltodextrin · Sodium Copper Chlorophyllin