Bronson

Yellow Round Tablet Vitamin & Mineral

Serving
1 Tablet(s)
Form
tablet
UPC
716563144012
DSLD
Formula hash
75f5518a70a2
Brand context
Catalog
659
products
With avoid flag
68
products
FDA recalls
0
history
CAERS
1
reports
Avoid-flaggedObjective label signals
Flagged excipients
1
1 avoid · 0 caution
FDA recalls
0
no recall history
CAERS reports
1
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

15 active ingredients
IngredientAmount% DV
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
200 mg333%
Vitamin D
vitaminUNII · 9VU1KI44GP
UL · set4 effects
100 IU25%
Thiamine
ThiaminvitaminUNII · X66NSO3N35
3 effects
20 mg1333%
Riboflavin
vitaminUNII · TLM2976OFR
5 effects
15 mg882%
Niacin
vitaminUNII · 2679MF687A
3 effects
2.9× ULexceeds NIH ODS adult upper limitsource →
100 mg500%
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
25 mg1250%
Biotin
vitaminUNII · 6SO6U10H04
3 effects
100 mcg33%
Pantothenic Acid
Pantothenic Acid (Vitamin B5)vitaminUNII · 19F5HK2737
30 mg300%
Zinc
mineralUNII · J41CSQ7QDS
UL · set8 effects
15 mg100%
Selenium
mineralUNII · H6241UJ22B
UL · set3 effects
25 mcg36%
Copper
mineralUNII · 789U1901C5
UL · set3 effects
1 mg50%
Manganese
mineralUNII · 42Z2K6ZL8P
UL · set2 effects
5 mg250%
Chromium
mineralUNII · 0R0008Q3JB
1 effect
25 mcg21%
Molybdenum
mineralUNII · 81AH48963U
UL · set1 effect
25 mcg33%
Potassium
mineralUNII · RWP5GA015D
3 effects
50 mg1%
What this product supports · authorized claims

25 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
1
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 · Stearic Acid · Croscarmellose Sodium · Magnesium Stearate · Silicon Dioxide · Hydroxypropyl Methylcellulose · Quercetin Dehydrate · FD&C #10 · FD&C #40 · Talc · Triacetin · Carnauba Wax