Home NDC 43742-0217 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 Ingredient Strength QUERCETIN 6 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 9IKM0I5T1E Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43742-0217-1 Quercetin 30 mL in 1 BOTTLE, DROPPER LIQUID 30 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-0217 QUERCETIN LIQUID [DESERET BIOLOGICALS, INC.] 5 Current NDC, Legacy NDC, 1 package rows 20240403_87dec202-711c-4270-a176-306cf6365558.zip
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43742-0217-1 43742021701 30 mL in 1 BOTTLE, DROPPER (43742-0217-1) 30 ml 2013-04-11 0000-00-00 No No Current