NOREPINEPHRINE PHENOLIC- norepinephrine (bitartrate) liquid 
Energique, 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 INGREDIENT:

(in each drop): 25% of Norepinephrine (Bitartrate) 6X, 12X, 30X; 12.50% of Norepinephrine (Bitartrate) 12C, 30C.

INDICATIONS:

May temporarily relieve symptoms associated with reactions to norepinephrine.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional.

Consult a physician for use in children under 12 years of age.

INDICATIONS:

May temporarily relieve symptoms associated with reactions to norepinephrine.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

Demineralized water, 20% Ethanol.

QUESTIONS:

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579   800.869.8078

PACKAGE LABEL DISPLAY:

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

NOREPINEPHRINE

PHENOLIC

1 fl. oz. (30 ml)

Norepinephrine Phenolic

NOREPINEPHRINE PHENOLIC 
norepinephrine (bitartrate) liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0499
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NOREPINEPHRINE BITARTRATE (UNII: IFY5PE3ZRW) (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:44911-0499-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product06/07/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic06/07/2019
Labeler - Energique, Inc. (789886132)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(44911-0499) , api manufacture(44911-0499) , label(44911-0499) , pack(44911-0499)

Revised: 3/2024
Document Id: caf1ecb8-e75e-45b0-a007-99de2afc618e
Set id: c5e6dda9-32c5-42f8-b302-b69ddbdb5011
Version: 4
Effective Time: 20240326
 
Energique, Inc.