Mineffect first aid antiseptic and antibiotic solution

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: Mineffect first aid antiseptic and antibiotic solution
Generic name: SILICEA, SULPHUR, PHOSPHORUS, CALCAREA SILICATA, NATRUM NITRICUM, FERRUM MURIATICUM, KALI SILICATUM
Manufacturer: Kadesh Incoporation Co,Ltd
Product type: HUMAN OTC DRUG
SPL set ID: 9bd266bb-7078-413f-8fc9-642353589130
SPL ID: 0906a804-bf9d-a63f-e063-6394a90a8e77
Version: 2
Effective date: 2023-10-31
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:27:55

Harmonized routes table
Harmonized routes
TOPICAL

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Mineffect first aid antiseptic and antibiotic solution	openfda.brand_name
generic name		SILICEA, SULPHUR, PHOSPHORUS, CALCAREA SILICATA, NATRUM NITRICUM, FERRUM MURIATICUM, KALI SILICATUM	openfda.generic_name
manufacturer name		Kadesh Incoporation Co,Ltd	openfda.manufacturer_name
ndc	package	81488-004-02	openfda.package_ndc
ndc	product	81488-004	openfda.product_ndc
ndc11	package	81488000402	derived:openfda.package_ndc
spl id		0906a804-bf9d-a63f-e063-6394a90a8e77	id
spl set id		9bd266bb-7078-413f-8fc9-642353589130	set_id
unii		27YLU75U4W	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		0I2XIN602U	openfda.unii
unii		8M4L3H2ZVZ	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		J86L1GUL6K	openfda.unii
unii		S4255P4G5M	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 Do not Use In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor When using this product *replace cap after using Stop use and ask a doctor *If condition worsens *If condition last more than 7 days or clear up and occur again within a few days If pregnant or breast-feeding, ask a health professional before use Keep out of reach of children

Reported adverse events (FAERS/openFDA)#

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