NOREPINEPHRINE - norepinephrine, liquid 
Apotheca Company

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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Norepinephrine

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 of 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 contact Poison Control Center right away.


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.


Dist. By:

Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com


PACKAGE LABEL DISPLAY:

DESBIO
NDC 57520-0804-1
HOMOPATHIC

NOREPINEPHRINE

1 FL OZ (30 ml)

Norepinephrine

NOREPINEPHRINE 
norepinephrine, liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57520-0804
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NOREPINEPHRINE (UNII: X4W3ENH1CV) (NOREPINEPHRINE - UNII:X4W3ENH1CV) NOREPINEPHRINE6 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57520-0804-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/22/201103/26/2017
Labeler - Apotheca Company (844330915)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(57520-0804) , api manufacture(57520-0804) , label(57520-0804) , pack(57520-0804)

Revised: 1/2016
 
Apotheca Company