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Sundown Naturals

Folic Acid Xtra

Serving
1 Caplet(s)
UPC
030768000080
DSLD
5805
Formula hash
73edde4c5a03
Brand context
Sundown Naturals
Catalog
776
products
With avoid flag
47
products
FDA recalls
0
history
CAERS
64
reports
Avoid-flaggedObjective label signals
Flagged excipients
3
1 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
37
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
60 mg100%
Riboflavin
vitaminUNII · TLM2976OFR
5 effects
25 mg1471%
Vitamin B6
vitaminUNII · KV2JZ1BI6Z
UL · set6 effects
25 mg1250%
Folate
vitaminUNII · 935E97BOY8
UL · set2 effects
800 mcg200%
Vitamin B12
vitaminUNII · 8406EY2OQA
3 effects
250 mcg4167%
Choline
vitaminUNII · N91BDP6H0X
UL · set3 effects
25 mg—
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

3 flagged · authority citations

  • ● AVOIDTitanium Dioxide color
    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 →
  • ◐ 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 →
FDA CAERS · adverse event context
37
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

Dextrose · Vegetable Cellulose · Silica · Vegetable Magnesium Stearate