DOCTOR INK TOPICAL ANTISEPTIC WITH PAIN RELIEF

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 INK TOPICAL ANTISEPTIC WITH PAIN RELIEF
Generic name: BENZALKONIUM CHLORIDE, LIDOCAINE
Manufacturer: Enviro Specialty Chemicals Inc
Product type: HUMAN OTC DRUG
SPL set ID: f7abe66c-dc2d-4ef7-9b11-5b87157fd302
SPL ID: 09dd7a4a-1a4a-4237-b72c-6ed735c73c36
Version: 3
Effective date: 2026-07-21
Source export date: 2026-10-12
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:32:36

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		DOCTOR INK TOPICAL ANTISEPTIC WITH PAIN RELIEF	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE, LIDOCAINE	openfda.generic_name
manufacturer name		Enviro Specialty Chemicals Inc	openfda.manufacturer_name
ndc	package	71884-204-04	openfda.package_ndc
ndc	package	71884-204-03	openfda.package_ndc
ndc	package	71884-204-01	openfda.package_ndc
ndc	package	71884-204-05	openfda.package_ndc
ndc	package	71884-204-02	openfda.package_ndc
ndc	product	71884-204	openfda.product_ndc
ndc11	package	71884020404	derived:openfda.package_ndc
ndc11	package	71884020403	derived:openfda.package_ndc
ndc11	package	71884020405	derived:openfda.package_ndc
ndc11	package	71884020402	derived:openfda.package_ndc
ndc11	package	71884020401	derived:openfda.package_ndc
rxcui		2629979	openfda.rxcui
spl id		09dd7a4a-1a4a-4237-b72c-6ed735c73c36	id
spl set id		f7abe66c-dc2d-4ef7-9b11-5b87157fd302	set_id
unii		98PI200987	openfda.unii
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.