Mycocan Combo

Manufacturer
Nutritional Specialties, Inc.
Effective date
2025-04-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:33:11

Label at a glance#

ProductMycocan Combo
Active ingredientCANDIDA ALBICANS
Label structure9 sections

Indications and uses

Aids in temporary relief of flatulence, bloating of the stomach, vaginal itching, and vaginal discharge.† †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage and administration

• Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. • Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Candida Albicans 12X, 30X, 60X, 100X, 500X.

PURPOSE:

OTC - PURPOSE SECTION

Candida Albicans - Assists in relief of flatulence, bloating, vaginal itching and vaginal discharge

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

USES:

INDICATIONS & USAGE SECTION

Aids in temporary relief of flatulence, bloating of the stomach, vaginal itching, and vaginal discharge.†

†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.

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

If condition worsens, seek medical attention.

KEEP OUT OF REACH OF CHILDREN

Do not use if tamper evident seal is broken or missing.

Store in a cool place after opening

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: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage.

• Do not take within 15 minutes of consuming food, beverage or brushing teeth.

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Alcohol USP 20%, Purified Water USP.

QUESTIONS:

OTC - QUESTIONS SECTION

MANUFACTURED EXCLUSIVELY FOR

NUTRITIONAL SPECIALTIES, INC.

PO BOX 97227

PITTSBURG, PA 15229

www.phpltd.com

1-800-245-1313

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Professional

Health Products

HOMEOPATHIC

NDC 83027-0061-1

MYCOCAN COMBO

2 FL. OZ (60 ml)

MYCOCAN COMBOMYCOCAN COMBO

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83027-0061-1Mycocan Combo60 mL in 1 BOTTLE, SPRAYSPRAY602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83027-0061MYCOCAN COMBO (CANDIDA ALBICANS) SPRAY [NUTRITIONAL SPECIALTIES, INC.]2Current NDC, 1 package rows20250409_45f22b37-4792-4d6d-a1b3-145b395eb448.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83027-006183027-0061-1

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
CANDIDA ALBICANS4D7G21HDBCACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

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
Mycocan ComboCANDIDA ALBICANSNutritional Specialties, Inc.45f22b37-4792-4d6d-a1b3-145b395eb4482025-04-07WarningsExact identifier
ndc (package): 83027-0061-1
ndc (product): 83027-0061
ndc11 (package): 83027006101
spl id: 13724a4a-eee4-4847-a1ad-f73faf1ebc98
spl set id: 45f22b37-4792-4d6d-a1b3-145b395eb448

Reported adverse events (FAERS/openFDA)#

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