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CVS Health

One Daily Essential

Serving
1 Tablet(s)
Per container
365
Form
tablet
UPC
050428434000
DSLD
278545
Avoid-flaggedObjective label signals
Flagged excipients
4
1 avoid · 3 caution
FDA recalls
0
no recall history
CAERS reports
13
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

12 active ingredients
IngredientAmount% DV
Vitamin A
UNII · 81G40H8B0T
3000 IU60%
Vitamin C
UNII · PQ6CK8PD0R
60 mg100%
Vitamin D
UNII · 9VU1KI44GP
400 IU100%
Vitamin E
UNII · H4N855PNZ1
30 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%
Pantothenic Acid
Pantothenic Acid (Vitamin B5)UNII · 19F5HK2737
10 mg100%
Calcium
UNII · SY7Q814VUP
45 mg5%
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.

    eur-lex.europa.eu →efsa.europa.eu →ecfr.gov →
  • ◐ CAUTIONFD&C Red #40 Aluminum 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 →
  • ◐ CAUTIONFD&C Yellow #6 Aluminum 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 →
  • ◐ CAUTIONFD&C Blue #2 Aluminum Lake
    color

    Banned from direct food use in Norway; restricted in EU under Commission Regulation 1333/2008. FDA permits under 21 CFR 74.102 with labeling requirement.

    eur-lex.europa.eu →
FDA CAERS · adverse event context
13
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

Calcium Carbonate · Ascorbic Acid · DL-Alpha-Tocopheryl Acetate · Gelatin · Niacinamide · Calcium Pantothenate · Dicalcium Phosphate · Calcium Silicate · Microcrystalline Cellulose · Crospovidone · Dextrin · Stearic Acid · Hypromellose · Pyridoxine Hydrochloride · Riboflavin · Thiamine Mononitrate · Polyethylene Glycol · Vitamin A Acetate · Dextrose · Magnesium Stearate · Lecithin · Folic Acid · Beta-Carotene · Cholecalciferol · Cyanocobalamin

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.