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Jarrow Formulas

Glucose Optimizer

Serving
2 Tablet(s)
Per container
30
Form
tablet
UPC
790011290025
DSLD
243280
Recall historyObjective label signals
Flagged excipients
0
none
FDA recalls
1
1 Class I / II
CAERS reports
18
FDA consumer events
Certifications
0
none recorded
1 FDA recall on file. · Every flag below links to the authority's published citation.

Supplement Facts

19 active ingredients
IngredientAmount% DV
Vitamin C
UNII · PQ6CK8PD0R
100 mg110%
Vitamin E
UNII · H4N855PNZ1
11 mg70%
Thiamine
ThiaminUNII · X66NSO3N35
5 mg420%
Niacin
UNII · 2679MF687A
8.6× ULexceeds NIH ODS adult upper limitsource →
300 mg1880%
Vitamin B6
UNII · KV2JZ1BI6Z
5 mg290%
Vitamin B12
UNII · 8406EY2OQA
100 mcg4170%
Biotin
UNII · 6SO6U10H04
1000 mcg3330%
Pantothenic Acid
Pantothenic Acid (Vitamin B5)UNII · 19F5HK2737
25 mg500%
Magnesium
UNII · I38ZP9992A
200 mg50%
Selenium
UNII · H6241UJ22B
10 mcg20%
Manganese
UNII · 42Z2K6ZL8P
1 mg40%
Chromium
UNII · 0R0008Q3JB
200 mcg570%
Glycostat Wild Bitter Melon extract
Bitter Melon
750 mg—
Gymnema sylvestre
Gymnema
300 mg—
Alpha Lipoic Acid
UNII · 73Y7P0K73Y
200 mg—
Eucalyptus leaf essential Oil Complex
Eucalyptus
100 mg—
Gamma Tocopherol
UNII · 8EF1Z1238F
100 mg—
Resveratrol
UNII · Q369O8926L
50 mg—
Banaba leaf extract
banabaUNII · OUK5B3W9E4
48 mg—
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.

Recall history

1 FDA recall

  1. Class II2018-01-15brand-level

    Jarrow Formulas Liquid L-Carnitine; 16 fl oz. (475 ml) bottle, dietary supplement; product number 102006; UPC 7 90011 02006 6; Vitamin B5 10 mg; L-Carnitine 1000 mg; Other ingredients: Purified water, xylitol, glycerin, citric acid, natural lemon-lime flavor, nisin (as a preservative). Distributed exclusively by Jarrow Formulas Los Angeles, CA.

    Reason: A higher than normal micro result was found at the six month time point for one lot of Liquid L-Carnitine.

    FDA record →
FDA CAERS · adverse event context
18
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

Cellulose · Calcium Phosphate · modified Food Starch · Magnesium Stearate · Silicon Dioxide · food-grade Coating

Chemically equivalent

Same formula, different brand

Products with identical sorted (ingredient, amount) tuples.