HISTAMINE- histaminum hydrochloricum liquid

Histamine by

Drug Labeling and Warnings

Histamine by is a Homeopathic medication manufactured, distributed, or labeled by Deseret Biologials, Inc., Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS: ​Histaminum Hydrochloricum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C

PURPOSE

​INDICATIONS: ​For temporary relief of hay fever, asthma, congestion, depression, fatigue, hives, hyperactivity, sinusitis and stomach discomfort.

WARNINGS

WARNINGS: Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

If pregnant or breast-feeding, seek advice of a health professional before use.

Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

DOSAGE & ADMINISTRATION

DIRECTIONS: 1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:​Demineralized Water, 25% Ethanol

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN. In case of overdose, contact physician or Poison Control Center right away.

INDICATIONS & USAGE

INDICATIONS: For temporary relief of hay fever, asthma, congestion, depression, fatigue, hives, hyperactivity, sinusitis and stomach discomfort.

QUESTIONS

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC: 43742-0086-1

HOMEOPATHIC

HISTAMINE

1 FL OZ (30 ml)

INGREDIENTS AND APPEARANCE

HISTAMINE 
histaminum hydrochloricum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43742-0086
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3)	HISTAMINE DIHYDROCHLORIDE	6 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43742-0086-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	08/16/2012	06/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/16/2012	06/23/2020

Labeler - Deseret Biologials, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(43742-0086)