Candida Combo

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-01-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:25:48

Label at a glance#

ProductCandida Combo
Active ingredientCANDIDA ALBICANS, ISSATCHENKIA ORIENTALIS WHOLE, CANDIDA PARAPSILOSIS
Label structure9 sections

Dosage and administration

Adults and children 15 drops orally, 2 times 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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 8.33% of Candida Albicans 15C, 18C, 27C, 36C, Candida Krusei 15C, 18C, 27C, 36C, Candida Parapsilosis 15C, 18C, 27C, 36C. 

INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of fatigue.** 

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

WARNINGS:

WARNINGS SECTION

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:

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 15 drops orally, 2 times 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:

INDICATIONS & USAGE SECTION

For temporary relief of fatigue.**

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

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 DISPLAY LABEL:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

CANDIDA

COMBO

1 fl. oz. (30 ml)

Candida ComboCandida Combo

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0544-12024-01-23C16284748780-1f386c64a-057a-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0544-12023-01-30C16284748780-1f386c64a-057a-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0544-1Candida Combo30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0544CANDIDA COMBO (CANDIDA ALBICANS, CANDIDA KRUSEI, CANDIDA PARAPSILOSIS) LIQUID [ENERGIQUE, INC.]3Current NDC, Legacy NDC, 1 package rows20240124_9a794fb7-db06-43bf-835c-b1807b3f9be0.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-054444911-0544-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML · Source PDF

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
Candida ComboCANDIDA ALBICANS, CANDIDA KRUSEI, CANDIDA PARAPSILOSISEnergique, Inc.9a794fb7-db06-43bf-835c-b1807b3f9be02024-01-23WarningsExact identifier
ndc (package): 44911-0544-1
ndc (product): 44911-0544
ndc11 (package): 44911054401
spl id: d4900e0d-4def-4030-af22-30b4355dbe55
spl set id: 9a794fb7-db06-43bf-835c-b1807b3f9be0

Reported adverse events (FAERS/openFDA)#

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