Home NDC 43742-0771 Melatonin
Product NDC 43742-0771
11-digit product format 437420771
Labeler code 43742
Product ID 43742-0771_43f1b593-3e12-4009-af39-7d4b35a291ea
Type HUMAN OTC DRUG
Nonproprietary name Melatonin
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2016-06-08
Substance MELATONIN
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 Melatonin
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MELATONIN 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 JL5DK93RCL 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 43742-0771-1 Melatonin 30 mL in 1 BOTTLE, DROPPER LIQUID 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-0771 MELATONIN LIQUID [DESERET BIOLOGICALS, INC.] 2 Current NDC, Legacy NDC, 1 package rows 20240402_4ea9b3dc-a6f7-48b0-b0a7-ac2951bc575d.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 43742-0771-1 43742077101 30 mL in 1 BOTTLE, DROPPER (43742-0771-1) 30 ml 2016-06-08 0000-00-00 No No Current