MICOX

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: MICOX
Generic name: ASPERGILLUS NIGER VAR. NIGER - CANDIDA ALBICANS - CENTELLA ASIATICA - MALIC ACID - MERCURIC CHLORIDE - RHIZOPUS STOLONIFER - SODIUM DIETHYL OXALACETATE - SULFUR - TABEBUIA IMPETIGINOSA BARK -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: 790b50d3-8e1e-4c36-be74-f30c51ca7895
SPL ID: 53f56dc9-eac1-51a5-e063-6394a90a896f
Version: 6
Effective date: 2026-06-11
Source export date: 2026-10-27
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:45:35

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		MICOX	openfda.brand_name
generic name		ASPERGILLUS NIGER VAR. NIGER - CANDIDA ALBICANS - CENTELLA ASIATICA - MALIC ACID - MERCURIC CHLORIDE - RHIZOPUS STOLONIFER - SODIUM DIETHYL OXALACETATE - SULFUR - TABEBUIA IMPETIGINOSA BARK -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-420-18	openfda.package_ndc
ndc	product	17089-420	openfda.product_ndc
ndc11	package	17089042018	derived:openfda.package_ndc
spl id		53f56dc9-eac1-51a5-e063-6394a90a896f	id
spl set id		790b50d3-8e1e-4c36-be74-f30c51ca7895	set_id
unii		7M867G6T1U	openfda.unii
unii		53GH7MZT1R	openfda.unii
unii		4D7G21HDBC	openfda.unii
unii		817L1N4CKP	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		FEE198DK4Q	openfda.unii
unii		6GLA1946WX	openfda.unii
unii		6CA025Y4FG	openfda.unii
unii		9IOA40ANG6	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS 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%

Reported adverse events (FAERS/openFDA)#

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