Member's Mark

Women's Daily Multivitamin

Serving

1 Tablet(s)

Per container

275

Form

tablet

UPC

193968030322

DSLD

272826

Avoid-flaggedObjective label signals

Flagged excipients

1 avoid · 2 caution

FDA recalls

no recall history

CAERS reports

FDA consumer events

Certifications

none recorded

1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

21 active ingredients

Ingredient	Amount	% DV
Vitamin A UNII · 81G40H8B0T	700 mcg	78%
Vitamin C UNII · PQ6CK8PD0R	75 mg	83%
Vitamin D3 Vitamin DUNII · 1C6V77QF41	25 mcg	125%
Vitamin E UNII · H4N855PNZ1	7.5 mg	50%
Vitamin K UNII · A034SE7857	25 mcg	21%
Thiamine ThiaminUNII · X66NSO3N35	1.2 mg	100%
Riboflavin UNII · TLM2976OFR	1.3 mg	100%
Niacin UNII · 2679MF687A	16 mg	100%
Vitamin B6 UNII · KV2JZ1BI6Z	1.7 mg	100%
Folate UNII · 935E97BOY8	680 mcg DFE	170%
Vitamin B12 UNII · 8406EY2OQA	6 mcg	250%
Biotin UNII · 6SO6U10H04	1000 mcg	3333%
Pantothenic Acid Pantothenic Acid (Vitamin B5)UNII · 19F5HK2737	5 mg	100%
Calcium UNII · SY7Q814VUP	380 mg	29%
Iron UNII · E1UOL152H7	18 mg	100%
Iodine UNII · 9679TC07X4	150 mcg	100%
Zinc UNII · J41CSQ7QDS	8 mg	73%
Selenium UNII · H6241UJ22B	27.5 mcg	50%
Copper UNII · 789U1901C5	0.9 mg	100%
Manganese UNII · 42Z2K6ZL8P	1.8 mg	78%
Chromium UNII · 0R0008Q3JB	25 mcg	71%

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 →
◐ CAUTIONButylated Hydroxytoluene
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 →
◐ 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

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 · Microcrystalline Cellulose · Starch · Ascorbic Acid · Ferrous Fumarate · Beta-Carotene · Biotin · Carboxymethylcellulose Sodium · Cholecalciferol · Chromium Chloride · Cupric Oxide · Cyanocobalamin · D-Calcium Pantothenate · DL-Alpha-Tocopherol · DL-Alpha-Tocopheryl Acetate · DL-Tartaric Acid · FD&C Blue #2 lake · FD&C Yellow #6 Lake · Folic Acid · Gelatin · Glucose · Gum Arabic · Hydroxypropylmethylcellulose · Magnesium Stearate · Maltodextrin · Manganese Sulfate · Medium Chain Triglyceride · Nicotinamide · Phytonadione · Polydextrose · Polyethylene Glycol · Polyvinyl Alcohol · Potassium Iodide · Pyridoxine Hydrochloride · Retinyl Acetate · Riboflavin · Silica · Sodium Aluminum Silicate · Sodium Ascorbate · Sodium Benzoate · Sodium Selenite · Sorbic Acid · Stearic Acid · Sugar · Sunflower Oil · Thiamine Mononitrate · Tocopherol · Tricalcium Phosphate · Zinc Oxide