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Nature's Blend

Super B Complex with Vitamin C

Serving
1 Capsule(s)
Per container
100
Form
capsule-unknown
UPC
079854200706
DSLD
274575
Formula hash
814478b1b342
Brand context
Nature's Blend
Catalog
195
products
With avoid flag
43
products
FDA recalls
0
history
CAERS
3
reports
Avoid-flaggedObjective label signals
Flagged excipients
3
1 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
2
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

6 active ingredients
IngredientAmount% DV
Vitamin C
vitaminUNII · PQ6CK8PD0R
UL · set5 effects
300 mg333%
Thiamine
ThiaminvitaminUNII · X66NSO3N35
3 effects
15 mg1250%
Riboflavin
vitaminUNII · TLM2976OFR
5 effects
10 mg769%
Niacin
vitaminUNII · 2679MF687A
3 effects
1.4× ULexceeds NIH ODS adult upper limitsource →
50 mg313%
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
5 mg294%
Pantothenic Acid
Pantothenic Acid (Vitamin B5)vitaminUNII · 19F5HK2737
10 mg200%
What this product supports · authorized claims

11 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

3 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
    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 →
  • ◐ 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.

    eur-lex.europa.eu →
FDA CAERS · adverse event context
2
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 · Magnesium Stearate · Silicon Dioxide · Croscarmellose Sodium

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.