Home NDC 43742-1729 BRUC HOMO
Product NDC 43742-1729
11-digit product format 437421729
Labeler code 43742
Product ID 43742-1729_d09f61f8-b7f4-49be-bcb5-e2e5353beb80
Type HUMAN OTC DRUG
Nonproprietary name Brucella Melitensis
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-10-02
Substance BRUCELLA MELITENSIS
Active strength 18 [hp_C]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base BRUC HOMO
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BRUCELLA MELITENSIS 18 [hp_C]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination OQF85710LZ 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 43742-1729-1 BRUC HOMO 30 mL in 1 BOTTLE, DROPPER LIQUID 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-1729 BRUC HOMO (BRUCELLA MELITENSIS) LIQUID [DESERET BIOLOGICALS, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20240425_916e818d-3f85-4020-ae9b-755d348576be.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 43742-1729-1 43742172901 30 mL in 1 BOTTLE, DROPPER (43742-1729-1) 30 ml 2020-10-02 0000-00-00 No No Current