Home NDC 43742-1935 MYCO HOMO
Product NDC 43742-1935
11-digit product format 437421935
Labeler code 43742
Product ID 43742-1935_2cb80b5f-80f2-4a24-84dc-fdc1333f2bf8
Type HUMAN OTC DRUG
Nonproprietary name Mycoplasma Pneumoniae
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-04-20
Substance MYCOPLASMA PNEUMONIAE
Active strength 15 [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 MYCO HOMO
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MYCOPLASMA PNEUMONIAE 15 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination JQE470FAD0 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 43742-1935-1 MYCO 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 43742-1935 MYCO HOMO (MYCOPLASMA PNEUMONIAE) LIQUID [DESERET BIOLOGICALS, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20240220_ce805acf-db0b-4b1f-ab3e-36bcb8cc1e57.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 43742-1935-1 43742193501 30 mL in 1 BOTTLE, DROPPER (43742-1935-1) 30 ml 2021-04-20 0000-00-00 No No Current