FDA.reportPublic FDA data

DRUG FACTS:

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2026-09-08
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-09-11 03:00:58

Label at a glance#

ProductCO Q 10
Active ingredientUBIDECARENONE
Label structure9 sections

Indications and uses

May temporarily relieve poor memory.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Individual responses may vary, and this product may not work for everyone.

Dosage and administration

• 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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): Ubidecarenonum 30X 100%.

PURPOSE:

OTC - PURPOSE SECTION

Ubidecarenonum - forgetfulness**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Individual responses may vary, and this product may not work for everyone.

USES:

INDICATIONS & USAGE SECTION

May temporarily relieve poor memory.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Individual responses may vary, and this product may not work for everyone.

WARNINGS:

WARNINGS SECTION

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:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

• 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:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.
201 Apple Blvd.
Woodbine, IA 51579

800.869.8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

CO Q 10

30X

1 fl. oz. (30 ml)

CO Q 10 30XCO Q 10 30X

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130363113600490GTIN-13: 0363113600490
EAN-13: 0363113600490
GTIN-12: 363113600490
UPC-A: 363113600490
GTIN storage (14 digits): 00363113600490		ENRG0549 CO Q 10 30X 1oz 9-8-26.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0339-12024-09-24C16284748780-1ba0f9c33-4eb0-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0339-12024-09-24C16284748780-1ba0f9c33-4eb0-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0339-12023-01-30C16284748780-1ba0f9c33-4eb0-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0339-12023-01-30C16284748780-1ba0f9c33-4eb0-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0339-12021-08-02C16284748780-1ba0f9c33-4eb0-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0339-12021-08-02C16284748780-1ba0f9c33-4eb0-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0339-12021-01-29C16284748780-1ba0f9c33-4eb0-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0339-12021-01-29C16284748780-1ba0f9c33-4eb0-a910-e053-dadaa90a0b85DRUG FACTS:

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-033944911-0339-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
UBIDECARENONEEJ27X76M46ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-09-24full-release2026-06-01 02:28:04

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CO Q 10UBIDECARENONUMEnergique, Inc.fd5e45ae-403f-44a2-abc0-343b9f550bdf2026-09-08WarningsExact identifier
ndc (package): 44911-0339-1
ndc (product): 44911-0339
ndc11 (package): 44911033901
spl id: 25ce4f34-9cb5-4af1-89de-f71ed9d71cea
spl set id: fd5e45ae-403f-44a2-abc0-343b9f550bdf

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.