NDC 43742-0086

Histamine

Histaminum Hydrochloricum

Histamine is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Deseret Biologials, Inc.. The primary component is Histamine Dihydrochloride.

• Product ID: 43742-0086_6c17a4ce-e598-4bfc-b8d1-462f3a6e81f2
• NDC: 43742-0086
• Product Type: Human Otc Drug
• Proprietary Name: Histamine
• Generic Name: Histaminum Hydrochloricum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2012-08-16
• Marketing End Date: 2020-06-23
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologials, Inc.
• Substance Name: HISTAMINE DIHYDROCHLORIDE
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0086-1

30 mL in 1 BOTTLE, DROPPER (43742-0086-1)

• Marketing Start Date: 2012-08-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0086-1 [43742008601]

Histamine LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-08-16
• Marketing End Date: 2020-06-23

Drug Details

Active Ingredients

Ingredient	Strength
HISTAMINE DIHYDROCHLORIDE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 5d75c211-d3cd-4b00-8bd1-e5e4f7d710c4
• Manufacturer:
  • Deseret Biologials, Inc.
• UNII:
  • 3POA0Q644U

NDC Crossover Matching brand name "Histamine" or generic name "Histaminum Hydrochloricum"

NDC	Brand Name	Generic Name
43742-0086	Histamine	Histaminum Hydrochloricum
43742-0696	Histamine	Histaminum Hydrochloricum
43857-0126	Histamine	Histaminum Hydrochloricum
43857-0309	Histamine	Histaminum Hydrochloricum
63083-1522	Histamine	Histamine
81701-111	ALEROFF	HISTAMINE
44911-0205	Histamine Phenolic	Histaminum Hydrochloricum
0220-2488	Histaminum 30C Allergy Relief	Histaminum Hydrochloricum
53645-1580	Histaminum Hydrochloricum	Histaminum Hydrochloricum
76472-3017	Histaminum Hydrochloricum	Histaminum Hydrochloricum
65044-9998	Positive Skin Test Control - Histamine	Histamine