Member's Mark

Glucosamine 1500 mg Chondroitin 1200 mg

Serving
2 Tablet(s)
Per container
100
Form
tablet
DSLD
Avoid-flaggedObjective label signals
Flagged excipients
3
1 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
15
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

5 active ingredients
IngredientAmount% DV
Calories
UNII · 1
15 {Calories}
Total Carbohydrates
CarbohydrateUNII · 0
2 Gram(s)1%
Sodium
UNII · 9NEZ333N27
130 mg5%
Glucosamine HCl
Glucosamine Hydrochloride
1500 mg
Chondroitin Sulfate
UNII · V5E8ELO4W9
1200 mg
Flagged excipients

3 flagged · authority citations

  • ● AVOIDTitanium Dioxide color
    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.

  • ◐ 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.

  • ◐ CAUTIONFD&C Yellow #5 Lake
    color

    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).

FDA CAERS · adverse event context
15
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

Cellulose · Croscarmellose · Povidone · Magnesium Silicate · Silica · Vegetable Magnesium Stearate