Quercetin

Product NDC
43742-0217
11-digit product format
437420217
Labeler code
43742
Product ID
43742-0217_698435a4-e0d8-4896-9e1d-69194ef3b34d
Type
HUMAN OTC DRUG
Nonproprietary name
Quercetin
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-04-11
Substance
QUERCETIN
Active strength
6 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Quercetin
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
QUERCETIN6 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9IKM0I5T1E

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-0217-1Quercetin30 mL in 1 BOTTLE, DROPPERLIQUID305

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
QUERCETINACTIVE INGREDIENT9IKM0I5T1EQUERCETIN LIQUID [DESERET BIOLOGICALS, INC.]3
QUERCETINACTIVE MOIETY9IKM0I5T1EQUERCETIN LIQUID [DESERET BIOLOGICALS, INC.]3
ALCOHOLINACTIVE INGREDIENT3K9958V90MQUERCETIN LIQUID [DESERET BIOLOGICALS, INC.]3
WATERINACTIVE INGREDIENT059QF0KO0RQUERCETIN LIQUID [DESERET BIOLOGICALS, INC.]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-0217QUERCETIN LIQUID [DESERET BIOLOGICALS, INC.]5Current NDC, Legacy NDC, 1 package rows20240403_87dec202-711c-4270-a176-306cf6365558.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-0217-14374202170130 mL in 1 BOTTLE, DROPPER (43742-0217-1) 30 ml2013-04-110000-00-00NoNoCurrent