Home NDC 43742-0696 Histamine
Product NDC 43742-0696
11-digit product format 437420696
Labeler code 43742
Product ID 43742-0696_3a9ff815-750d-4247-970e-0620b5d44ddc
Type HUMAN OTC DRUG
Nonproprietary name Histaminum Hydrochloricum
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologials, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-12-09
Substance HISTAMINE DIHYDROCHLORIDE
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 Histamine
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HISTAMINE DIHYDROCHLORIDE 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 3POA0Q644U 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 43742-0696-1 Histamine 30 mL in 1 BOTTLE, DROPPER LIQUID 30 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-0696 HISTAMINE (HISTAMINUM HYDROCHLORICUM) LIQUID [DESERET BIOLOGIALS, INC.] 5 Current NDC, Legacy NDC, 1 package rows 20240316_f1503ad8-cb3b-4de5-a07c-57e5b80b756f.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 43742-0696-1 43742069601 30 mL in 1 BOTTLE, DROPPER (43742-0696-1) 30 ml 2015-12-09 0000-00-00 No No Current