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
IngredientStrength
MELATONIN6 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiJL5DK93RCL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-0771-1Melatonin30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-0771MELATONIN LIQUID [DESERET BIOLOGICALS, INC.]2Current NDC, Legacy NDC, 1 package rows20240402_4ea9b3dc-a6f7-48b0-b0a7-ac2951bc575d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-0771-14374207710130 mL in 1 BOTTLE, DROPPER (43742-0771-1) 30 ml2016-06-080000-00-00NoNoCurrent