HISTAMINE- histaminum hydrochloricum liquid
Deseret Biologials, Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Histamine

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

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

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.

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 INGREDIENTS:Demineralized Water, 25% Ethanol

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

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

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)

Histamine

HISTAMINE
histaminum hydrochloricum liquid

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

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

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

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

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

Labeler - Deseret Biologials, Inc. (940741853)

Registrant - Apotheca Company (844330915)

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

Revised: 11/2018

Document Id: 6c17a4ce-e598-4bfc-b8d1-462f3a6e81f2

Set id: 5d75c211-d3cd-4b00-8bd1-e5e4f7d710c4

Version: 2

Effective Time: 20181106

Deseret Biologials, Inc.