Solgar

Solovite Iron-Free

Serving
1 Tablet(s)
Form
tablet
UPC
033984026223
DSLD
Avoid-flaggedObjective label signals
Flagged excipients
1
1 avoid · 0 caution
FDA recalls
0
no recall history
CAERS reports
41
FDA consumer events
Certifications
0
none recorded
1 avoid-level excipient · Every flag below links to the authority's published citation.

Supplement Facts

28 active ingredients
IngredientAmount% DV
Vitamin A
UNII · 81G40H8B0T
5000 IU100%
Vitamin C
UNII · PQ6CK8PD0R
150 mg250%
Vitamin D
UNII · 9VU1KI44GP
400 IU100%
Vitamin E
UNII · H4N855PNZ1
150 IU500%
Thiamine
ThiaminUNII · X66NSO3N35
25 mg1667%
Riboflavin
UNII · TLM2976OFR
25 mg1471%
Niacin
UNII · 2679MF687A
2.9× ULexceeds NIH ODS adult upper limitsource →
100 mg500%
Vitamin B6
UNII · KV2JZ1BI6Z
25 mg1250%
Folate
UNII · 935E97BOY8
100 mcg25%
Vitamin B12
UNII · 8406EY2OQA
100 mcg1667%
Biotin
UNII · 6SO6U10H04
20 mcg7%
Pantothenic Acid
Pantothenic Acid (Vitamin B5)UNII · 19F5HK2737
50 mg500%
Calcium
UNII · SY7Q814VUP
30 mg3%
Iron
UNII · E1UOL152H7
0 mg0%
Phosphorus
UNII · 27YLU75U4W
13 mg1%
Iodine
UNII · 9679TC07X4
100 mcg67%
Magnesium
UNII · I38ZP9992A
0.4 mg1%
Zinc
UNII · J41CSQ7QDS
0.18 mg1%
Manganese
UNII · 42Z2K6ZL8P
0.7 mg35%
Citrus Bioflavonoids
Flavonoid (mixture)UNII · BD70459I50
25 mg
Betaine HCl
Betaine HydrochlorideUNII · 3SCV180C9W
25 mg
Inositol
UNII · 4L6452S749
25 mg
Rutin
UNII · 5G06TVY3R7
25 mg
Choline
UNII · N91BDP6H0X
10 mg
Lysine
UNII · K3Z4F929H6
10 mg
Hesperidin Complex
Blend (non-nutrient/non-botanical)
5 mg
Carotenoid Mix
carotenoids
29 mcg
Natural Powdered Blend
Blend (Combination)
7 mg
What this product supports · authorized claims

28 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

1 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.

FDA CAERS · adverse event context
41
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 · Vegetable Cellulose · Silica · Stearic Acid · Vegetable Glycerin · Chlorophyll