supplementhackr
Major

Tab A Vite Multiple Vitamins

Serving
1 Tablet(s)
Form
tablet
UPC
309040530806
DSLD
201749
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

9 active ingredients
IngredientAmount% DV
Vitamin A
UNII · 81G40H8B0T
5000 IU100%
Vitamin C
UNII · PQ6CK8PD0R
60 mg100%
Vitamin D3
Vitamin DUNII · 1C6V77QF41
400 IU100%
Thiamine
ThiaminUNII · X66NSO3N35
1.5 mg100%
Riboflavin
UNII · TLM2976OFR
1.7 mg100%
Niacin
UNII · 2679MF687A
20 mg100%
Vitamin B6
UNII · KV2JZ1BI6Z
2 mg100%
Folate
UNII · 935E97BOY8
400 mcg100%
Vitamin B12
UNII · 8406EY2OQA
6 mcg100%
What this product supports · authorized claims

15 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 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 →
  • ◐ CAUTIONBHT
    preservative

    NTP 15th Report on Carcinogens (2021) classifies BHT/BHA as not listed, but BHA is 'reasonably anticipated to be a human carcinogen'. EU permits BHT with strict limits under Commission Regulation 1333/2008 Annex II.

    ntp.niehs.nih.gov →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

Sugar · Dicalcium Phosphate · Calcium Sulfate · Kaolin · Magnesium Silicate · Microcrystalline Cellulose · Stearic Acid · Gelatin · Starch · Croscarmellose Sodium · Pharmaceutical Glaze · Sodium Ascorbate · Triglycerides · Silica · Mixed Tocopherols · Carnauba Wax

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.