CVS Health

Prenatal Vitamins

Serving

1 Tablet(s)

Form

tablet

UPC

050428357422

DSLD

239462

Avoid-flaggedObjective label signals

Flagged excipients

1 avoid · 3 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

13 active ingredients

Ingredient	Amount	% DV
Vitamin A UNII · 81G40H8B0T	4000 IU	50%
Vitamin C UNII · PQ6CK8PD0R	100 mg	167%
Vitamin D3 Vitamin DUNII · 1C6V77QF41	400 IU	100%
Vitamin E UNII · H4N855PNZ1	11 IU	37%
Thiamine ThiaminUNII · X66NSO3N35	1.5 mg	88%
Riboflavin UNII · TLM2976OFR	1.7 mg	85%
Niacin UNII · 2679MF687A	18 mg	90%
Vitamin B6 UNII · KV2JZ1BI6Z	2.6 mg	104%
Folate UNII · 935E97BOY8	800 mcg	100%
Vitamin B12 UNII · 8406EY2OQA	4 mcg	50%
Calcium UNII · SY7Q814VUP	263 mg	26%
Iron UNII · E1UOL152H7	27 mg	150%
Zinc UNII · J41CSQ7QDS	25 mg	167%

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 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 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 →
◐ 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

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

Microcrystalline Cellulose · Stearic Acid · Hypromellose · Croscarmellose Sodium · Gelatin · Acacia · Maltodextrin · Talc · Triacetin · Starch · Magnesium Stearate · Dicalcium Phosphate · Mineral Oil · Sucrose · Silica · Sodium Ascorbate · Triglycerides · Tocopherols · Sodium Benzoate · Sorbic Acid · Tricalcium Phosphate · Ascorbyl Palmitate

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.