Rugby

Lipogen

Serving
3 Softgel Capsule(s)
Per container
20
Form
capsule-unknown
UPC
00536-3908-086
DSLD
Avoid-flaggedObjective label signals
Flagged excipients
4
1 avoid · 3 caution
FDA recalls
0
no recall history
CAERS reports
7
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

9 active ingredients
IngredientAmount% DV
Vitamin C
UNII · PQ6CK8PD0R
300 mg500%
Thiamine
ThiaminUNII · X66NSO3N35
1 mg67%
Riboflavin
UNII · TLM2976OFR
1 mg59%
Niacin
UNII · 2679MF687A
10 mg50%
Vitamin B6
UNII · KV2JZ1BI6Z
1 mg50%
Vitamin B12
UNII · 8406EY2OQA
5 mcg83%
Pantothenic Acid
Pantothenic Acid (Vitamin B5)UNII · 19F5HK2737
5 mg50%
Sodium
UNII · 9NEZ333N27
15 mg1%
Choline Bitartrate
CholineUNII · 6K2W7T9V6Y
334 mg
What this product supports · authorized claims

13 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.

  • ◐ CAUTIONFD&C Red #40
    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).

  • ◐ CAUTIONFD&C yellow # 6
    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 Blue #1
    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.

FDA CAERS · adverse event context
7
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

Soybean Oil · Gelatin · Palm Oil · Glycerin · Soy Lecithin · purified Water · yellow Beeswax · Lemon Bioflavonoids · dicalcium phosphate anhydrous · Inositol · Lemon Oil · Ethyl Vanillin