NOREPINEPHRINE- norepinephrine liquid
Deseret Biologicals, 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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Drug Facts:

ACTIVE INGREDIENTS:

Norepinephrine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

INDICATIONS:

For temporary relief of symptoms related to Norepinephrine sensitivity including rashes, hypertension, hives, Premenstrual Syndrome, tachycardia, headache, hot flashes, Seasonal Affective Disorder, sleep disorders and blurred vision.

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:

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

INDICATIONS:

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0101-1

HOMEOPATHIC

NOREPINEPHRINE

1 FL OZ (30 ml)

NOREPINEPHRINE

NOREPINEPHRINE
norepinephrine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0101
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
NOREPINEPHRINE (UNII: X4W3ENH1CV) (NOREPINEPHRINE - UNII:X4W3ENH1CV)	NOREPINEPHRINE	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:43742-0101-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	08/24/2012	08/19/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		08/24/2012	08/19/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0101) , api manufacture(43742-0101) , label(43742-0101) , pack(43742-0101)

Revised: 3/2017

Document Id: 48e256d2-a64d-4eaf-ba2a-9370f61f5c32

Set id: d65fb844-183c-462f-a4ce-200ca5fe0803

Version: 2

Effective Time: 20170317

Deseret Biologicals, Inc.