QUERCETIN PHENOLIC- quercetin, 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): 33.33% of Quercetin 6X; 16.67% of Quercetin 12X, 30X, 12C, 30C.

INDICATIONS:

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

**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.

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.

INACTIVE INGREDIENTS:

Demineralized water, 20% Ethanol.

KEEP OUT OF REACH OF CHILDREN:

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

INDICATIONS:

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

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

QUESTIONS:

Dist. by Energique, Inc.

201 Apple Blvd.

Woodbine, IA 51579  800.869.8078

PACKAGE LABEL DISPLAY:

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

QUERCETIN

PHENOLIC

1 fl. oz. (30 ml)

Quercetin Phenolic

QUERCETIN PHENOLIC 
quercetin, liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0013
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
QUERCETIN (UNII: 9IKM0I5T1E) (QUERCETIN - UNII:9IKM0I5T1E) QUERCETIN6 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:44911-0013-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product06/05/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic06/05/2012
Labeler - Energique, Inc. (789886132)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(44911-0013) , api manufacture(44911-0013) , label(44911-0013) , pack(44911-0013)

Revised: 3/2024
Document Id: 93d52df0-1631-4041-95b2-51ad3dba828a
Set id: be0e5c01-7e28-4de4-abce-e40ae27bdb41
Version: 4
Effective Time: 20240326
 
Energique, Inc.