supplementhackr
Rugby

B Complex

Serving
1 Softgel Capsule(s)
Form
capsule-unknown
UPC
00536-4787-017
DSLD
28353
Avoid-flaggedObjective label signals
Flagged excipients
4
1 avoid · 3 caution
FDA recalls
0
no recall history
CAERS reports
8
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

8 active ingredients
IngredientAmount% DV
Thiamine
ThiaminUNII · X66NSO3N35
3 mg200%
Riboflavin
UNII · TLM2976OFR
3 mg176%
Niacin
UNII · 2679MF687A
20 mg100%
Vitamin B6
UNII · KV2JZ1BI6Z
0.5 mg25%
Vitamin B12
UNII · 8406EY2OQA
1 mcg17%
Pantothenic Acid
Pantothenic Acid (Vitamin B5)UNII · 19F5HK2737
5 mg50%
desiccated Liver
Liver
60 mg—
Debittered Brewer's Yeast
Brewer's Yeast
60 mg—
What this product supports · authorized claims

9 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

4 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.

    eur-lex.europa.eu →efsa.europa.eu →ecfr.gov →
  • ◐ CAUTIONFD&C Red #40 Lake
    color

    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 #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.

    eur-lex.europa.eu →
  • ◐ CAUTIONFD&C blue #1 lake
    color

    EU requires 'attention in children' warning per Commission Regulation 1333/2008 Annex III. Limited to specific food categories; capsule-shell use permitted with restrictions.

    eur-lex.europa.eu →
FDA CAERS · adverse event context
8
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 · Soybean Oil · Glycerin · purified Water · Sunflower Lecithin · Beeswax · Dicalcium Phosphate