ACONITE- aconitum napellus 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): 100% of Aconitum Napellus 200C.

INDICATIONS:

May temporarily relieve sudden onset of illness with intense pain.**

**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:

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 sudden onset of illness with intense pain.**

**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

ACONITE 200C

1 fl. oz. (30 ml)

ACONITE 200C

ACONITE 
aconitum napellus liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0209
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS WHOLE200 [hp_C]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:44911-0209-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product07/15/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/15/2015
Labeler - ENERGIQUE, INC. (789886132)
Registrant - APOTHECA COMPANY (844330915)
Establishment
NameAddressID/FEIBusiness Operations
APOTHECA COMPANY844330915manufacture(44911-0209) , api manufacture(44911-0209) , label(44911-0209) , pack(44911-0209)

Revised: 6/2023
Document Id: 04259ae1-7e7d-4018-9866-9b0f378b2cfc
Set id: e5f8aa8c-0764-49e8-a2b1-4b8291eef882
Version: 4
Effective Time: 20230607
 
ENERGIQUE, INC.