Home NDC 0220-2467 Histaminum hydrochloricum
Product NDC 0220-2467
11-digit product format 002202467
Labeler code 0220
Product ID 0220-2467_42b2904a-1127-85c6-e063-6394a90afd78
Type HUMAN OTC DRUG
Nonproprietary name HISTAMINE DIHYDROCHLORIDE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance HISTAMINE DIHYDROCHLORIDE
Active strength 6 [hp_C]/6[hp_C]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Histaminum hydrochloricum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HISTAMINE DIHYDROCHLORIDE 6 [hp_C]/6[hp_C]
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 0220-2467-41 Histaminum hydrochloricum 6 [hp_C] in 1 TUBE PELLET 6 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-2467 HISTAMINUM HYDROCHLORICUM (HISTAMINE DIHYDROCHLORIDE ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20230121_85b7ee33-d037-afe8-e053-2991aa0a681b.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 Marketing start Marketing end Sample Exclude flag Status 0220-2467-41 00220246741 6 [hp_C] in 1 TUBE (0220-2467-41) 1983-03-03 0000-00-00 No No Current