DOCTOR INKS TOPICAL ANTISEPTIC

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: DOCTOR INKS TOPICAL ANTISEPTIC
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Enviro Specialty Chemicals Inc
Product type: HUMAN OTC DRUG
SPL set ID: d503a2db-e326-4a31-bc6a-5034ad74bf0b
SPL ID: 1984543f-4ded-41ba-acf8-5e3813680672
Version: 3
Effective date: 2026-07-21
Source export date: 2026-10-27
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:58:55

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		DOCTOR INKS TOPICAL ANTISEPTIC	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Enviro Specialty Chemicals Inc	openfda.manufacturer_name
ndc	package	71884-203-03	openfda.package_ndc
ndc	package	71884-203-01	openfda.package_ndc
ndc	package	71884-203-04	openfda.package_ndc
ndc	package	71884-203-02	openfda.package_ndc
ndc	package	71884-203-05	openfda.package_ndc
ndc	product	71884-203	openfda.product_ndc
ndc11	package	71884020303	derived:openfda.package_ndc
ndc11	package	71884020304	derived:openfda.package_ndc
ndc11	package	71884020305	derived:openfda.package_ndc
ndc11	package	71884020301	derived:openfda.package_ndc
ndc11	package	71884020302	derived:openfda.package_ndc
rxcui		1098199	openfda.rxcui
spl id		1984543f-4ded-41ba-acf8-5e3813680672	id
spl set id		d503a2db-e326-4a31-bc6a-5034ad74bf0b	set_id
unii		F5UM2KM3W7	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 FREEZE. FOR EXTERNAL USE ONLY. DO NOT USE IN EARS, EYES OR MOUTH. When using this product, avoid contact with the eyes. In case of contact, flush eyes with water. Stop use and ask a doctor if redness or irritation develops and persists for more than 72 hours. Keep out of reach of children. Children should be supervised when using this product.

Reported adverse events (FAERS/openFDA)#

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