0220-2488 NDC - HISTAMINUM 30C ALLERGY RELIEF (HISTAMINUM HYDROCHLORICUM)

Drug Information

Product NDC: 0220-2488
Proprietary Name: Histaminum 30C Allergy Relief
Non Proprietary Name: Histaminum Hydrochloricum
Active Ingredient(s): 30 [hp_C]/1 HISTAMINE DIHYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): PELLET

Labeler Information

Field Name	Field Value
Labeler Name:	Laboratoires Boiron
Product Type:	HUMAN OTC DRUG
FDA Application Number:
Marketing Category:	UNAPPROVED HOMEOPATHIC
Start Marketing Date:	3/17/2016

Package Information

No.	Package Code	Package Description	Billing Unit
1	0220-2488-41	80 PELLET in 1 TUBE (0220-2488-41)
2	0220-2488-43	3 TUBE in 1 PACKAGE (0220-2488-43) / 80 PELLET in 1 TUBE

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	0220-2488	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	HUMAN OTC DRUG	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAME	Histaminum 30C Allergy Relief	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
NON PROPRIETARY NAME	Histaminum Hydrochloricum	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	PELLET	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	ORAL	Name of Company corresponding to the labeler code segment of the Product NDC.
START MARKETING DATE	3/17/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	UNAPPROVED HOMEOPATHIC	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Laboratoires Boiron	This is the date that the labeler indicates was the start of its marketing of the drug product.
SUBSTANCE NAME	HISTAMINE DIHYDROCHLORIDE	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	30
ACTIVE INGRED UNIT	[hp_C]/1

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 12/6/2025