MICOX

Manufacturer
Guna spa
Effective date
2026-06-11
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
daily-update
Hydrated at
2026-06-13 05:10:07

Label at a glance#

ProductMICOX
Active ingredientASPERGILLUS NIGER VAR. NIGER, CANDIDA ALBICANS, MALIC ACID, CENTELLA ASIATICA, MERCURIC CHLORIDE, RHIZOPUS STOLONIFER, SODIUM DIETHYL OXALACETATE, TABEBUIA IMPETIGINOSA BARK, SULFUR
Label structure10 sections

Indications and uses

Temporary relief of symptoms related to fungal infection of skin skin and mucosa, such as: Skin rash, r edness, itching mucosal redness, swelling Intestinal gas and bloating

Dosage and administration

Adults and children 12 years and older 20 drops in a little water, 2 times per day Children between 12 years and 6 years of age 10 drops in a little water, 2 times per day Children under 6 years 5 drops consult a physician

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS/PURPOSE

OTC - ACTIVE INGREDIENT SECTION

ASPERGILLUS NIGER 12X, 30X, 200X Immune support and detoxification

CANDIDA ALBICANS 12X, 30X, 200X Immune support and detoxification

DL-MALIC ACID 6X,12X, 30X Promotes cell metabolism


HYDROCOTYLE ASIATICA 6X Itching

MERCURIUS CORROSIVUS 6X Relieve skin and mucosa inflammation

MUCOR MUCEDO 12X, 30X, 200X Immune support and detoxification

NATRUM OXALACETICUM 6X,12X, 30X Promotes cell metabolism

PINK TRUMPET TREE 4X Relieve skin and mucosa inflammation

SULPHUR 6X Relieve skin and mucosa inflammation

USES

OTC - PURPOSE SECTION

Temporary relief of symptoms related to fungal infection of skin skin and mucosa, such as:

  • Skin rash, r edness, itching
  • mucosal redness, swelling
  • Intestinal gas and bloating

WARNINGS

WARNINGS SECTION

  • Stop use and ask doctor if symptoms persist more than 5 days.
  • 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.
  • Contains ethyl alcohol 30%

PREGNANCY

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding ask a doctor before use

WARNINGS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and older 20 drops in a little water, 2 times per day



Children between 12 years and 6 years of age 10 drops in a little water, 2 times per day



Children under 6 years 5 drops consult a physician

QUESTIONS

OTC - QUESTIONS SECTION

Questions?: info@gunainc.com, tel. (484) 223-3500

INACTIVE INGREDIENT SECTION

Inactive ingredient: Ethyl alcohol 30%.

INDICATIONS & USAGE SECTION

Take 15 minutes before meals.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5USMIC5USMIC

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix5USMIC5USMIC.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17089-420-182020-03-13C16284748780-19d75b9d0-c3c7-f424-e053-dadaa90a57ceMICOX
17089-420-182020-03-13C16284748780-19d75b9d0-c3c7-f424-e053-dadaa90a57ceMICOX
17089-420-182020-01-31C16284748780-19d75b9d0-c3c7-f424-e053-dadaa90a57ceMICOX
17089-420-182020-01-31C16284748780-19d75b9d0-c3c7-f424-e053-dadaa90a57ceMICOX

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ASPERGILLUS NIGER VAR. NIGERACTIVE INGREDIENT9IOA40ANG61
CANDIDA ALBICANSACTIVE INGREDIENT4D7G21HDBC1
CENTELLA ASIATICAACTIVE INGREDIENT7M867G6T1U1
MALIC ACIDACTIVE INGREDIENT817L1N4CKP1
MERCURIC CHLORIDEACTIVE INGREDIENT53GH7MZT1R1
RHIZOPUS STOLONIFERACTIVE INGREDIENTFEE198DK4Q1
SODIUM DIETHYL OXALACETATEACTIVE INGREDIENT6CA025Y4FG1
SULFURACTIVE INGREDIENT70FD1KFU701
TABEBUIA IMPETIGINOSA BARKACTIVE INGREDIENT6GLA1946WX1
ASPERGILLUS NIGER VAR. NIGERACTIVE MOIETY9IOA40ANG61
CANDIDA ALBICANSACTIVE MOIETY4D7G21HDBC1
CENTELLA ASIATICAACTIVE MOIETY7M867G6T1U1
DIETHYL OXALACETATEACTIVE MOIETY15S56468G71
MALIC ACIDACTIVE MOIETY817L1N4CKP1
MERCURIC CATIONACTIVE MOIETYED30FJ8Y421
RHIZOPUS STOLONIFERACTIVE MOIETYFEE198DK4Q1
SULFURACTIVE MOIETY70FD1KFU701
TABEBUIA IMPETIGINOSA BARKACTIVE MOIETY6GLA1946WX1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17089-42017089-420-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52022-11-15full-release2026-06-01 02:18:33

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 22 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates

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
MICOXASPERGILLUS NIGER VAR. NIGER - CANDIDA ALBICANS - CENTELLA ASIATICA - MALIC ACID - MERCURIC CHLORIDE - RHIZOPUS STOLONIFER - SODIUM DIETHYL OXALACETATE - SULFUR - TABEBUIA IMPETIGINOSA BARK -Guna spa790b50d3-8e1e-4c36-be74-f30c51ca78952026-06-11WarningsExact identifier
ndc (package): 17089-420-18
ndc (product): 17089-420
ndc11 (package): 17089042018
spl id: 53f56dc9-eac1-51a5-e063-6394a90a896f
spl set id: 790b50d3-8e1e-4c36-be74-f30c51ca7895

Reported adverse events (FAERS/openFDA)#

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