Nature's Measure

Women's Essential Vitamins

Serving
1 Tablet(s)
Form
tablet
UPC
311845343680
DSLD
Avoid-flaggedObjective label signals
Flagged excipients
3
1 avoid · 2 caution
FDA recalls
0
no recall history
CAERS reports
1
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
2000 IU40%
Vitamin C
UNII · PQ6CK8PD0R
10 mg17%
Vitamin D3
Vitamin DUNII · 1C6V77QF41
400 IU100%
Vitamin E
UNII · H4N855PNZ1
12.5 IU42%
Thiamine Mononitrate
ThiaminUNII · 8K0I04919X
1.5 mg100%
Riboflavin
UNII · TLM2976OFR
1.7 mg100%
Niacinamide
NiacinUNII · 25X51I8RD4
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%
Iron
UNII · E1UOL152H7
18 mg100%
What this product supports · authorized claims

17 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.

  • ◐ 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).

  • ◐ 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.

FDA CAERS · adverse event context
1
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

Dicalcium Phosphate · Stearic Acid · Croscarmellose Sodium · Gelatin · Starch · Silica · Microcrystalline Cellulose · Magnesium Stearate · Hypromellose · Magnesium Silicate · Sucrose · Polyethylene Glycol · Polyvinylpyrrolidone · mineral oil · Mixed Tocopherols · Glucose · Sodium Benzoate · Sorbic Acid

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.