AURUM MET- aurum metallicum 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.

----------

DRUG FACTS:

ACTIVE INGREDIENT:

(in each drop) Aurum Metallicum 200C 100%.

PURPOSES:

Aurum Metallicum - melancholy**

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

USES:

May temporarily relieve:  •melancholy  •hopelessness**

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

WARNINGS:

Stop use and ask a doctor if symptoms persist for more than 7 days.

If pregnant or breastfeeding, 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.

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

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

AURUM MET

200C

1 fl. oz. (30 ml)

AURUM MET 200C

AURUM MET 
aurum metallicum liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0380
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD200 [hp_C]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:44911-0380-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product08/16/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic08/16/2016
Labeler - Energique, Inc. (789886132)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(44911-0380) , api manufacture(44911-0380) , label(44911-0380) , pack(44911-0380)

Revised: 9/2024
Document Id: 27858e7d-6b7a-4f67-9f94-22a6d4a995d9
Set id: 9d7de1b6-8d5e-4881-9511-4723736a5abf
Version: 5
Effective Time: 20240923
 
Energique, Inc.