FDA.reportPublic FDA data

Quercetin

Manufacturer
Apotheca Company
Effective date
2022-11-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:48:11

Label at a glance#

ProductQuercetin
Active ingredientQUERCETIN
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS:  Quercetin 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

OTC - PURPOSE SECTION

INDICATIONS:  For temporary relief of symptoms related to food and pollen sensitivities including fatigue, headache, runny nose and congestion, itching eyes, diarrhea, bloating, and cramps.

WARNINGS SECTION

WARNINGS:  Keep out of reach of children.  In case of overdose, contact physician or Poison Control Center right away.

If pregnant or breast-feeding, seek advice of a health professional before use.

Tamper seal:  "Sealed for Your Protection."  Do not use if seal is broken or missing.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS:  1-10 drops under the tongue, 3 times a day or as directed by a health professional.  Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS:  Demineralized water, 25% Ethanol.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.  In case of overdose, contact physician or Poison Control Center right away.

INDICATIONS & USAGE SECTION

INDICATIONS:  For temporary relief of symptoms related to food and pollen sensitivities including fatigue, headache, runny nose and congestion, itching eyes, diarrhea, bloating, and cramps.

OTC - QUESTIONS SECTION

Dist. By:

Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 57520-1003-1

HOMEOPATHIC

QUERCETIN

1 FL OZ (30 ml)

QuercetinQuercetin

QuercetinQuercetin

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57520-1003-12022-11-14C16284748780-19d75b9d0-3061-f424-e053-dadaa90a57ceQuercetin
57520-1003-12020-01-31C16284748780-19d75b9d0-3061-f424-e053-dadaa90a57ceQuercetin

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
QUERCETINACTIVE INGREDIENT9IKM0I5T1E1
QUERCETINACTIVE MOIETY9IKM0I5T1E1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57520-100357520-1003-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
QUERCETIN9IKM0I5T1EACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
68a6c862-4004-491c-b87e-8660f9e7d2d1f8bd067b-49f3-4c06-82a3-7189cd3f573b2022-11-14WarningsExact identifier
spl id: 68a6c862-4004-491c-b87e-8660f9e7d2d1
spl set id: f8bd067b-49f3-4c06-82a3-7189cd3f573b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.