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Trigen Laboratories

Vol-Care Rx

Serving
1 Tablet(s)
Per container
100
Form
tablet
UPC
313811515107
DSLD
206674
Formula hash
1d7cde33c592
Brand context
Trigen Laboratories
Catalog
38
products
With avoid flag
23
products
FDA recalls
0
history
CAERS
1
reports
Avoid-flaggedObjective label signals
Flagged excipients
2
1 avoid · 1 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

9 active ingredients
IngredientAmount% DV
Folate
vitaminUNII · 935E97BOY8
UL · set2 effects
1 mg250%
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
10 mg500%
Thiamine
ThiaminvitaminUNII · X66NSO3N35
3 effects
1.5 mg100%
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
6 mcg100%
Riboflavin
vitaminUNII · TLM2976OFR
5 effects
1.7 mg100%
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
60 mg100%
Biotin
vitaminUNII · 6SO6U10H04
3 effects
300 mcg100%
Niacinamide
NiacinvitaminUNII · 25X51I8RD4
UL · set3 effects
20 mg100%
Pantothenic Acid
Pantothenic Acid (Vitamin B5)vitaminUNII · 19F5HK2737
10 mg100%
What this product supports · authorized claims

12 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

2 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 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).

    eur-lex.europa.eu →ecfr.gov →
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

Microcrystalline Cellulose · pregelatinized Starch · Dicalcium Phosphate · Polyvinyl Alcohol · silicified Microcrystalline Cellulose · Tripotassium Citrate · Citric Acid · Croscarmellose Sodium · Stearic Acid · Polyethylene Glycol · Talc

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.