DOCTOR INKS HAND SANITIZER

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 HAND SANITIZER
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Enviro Specialty Chemicals Inc
Product type: HUMAN OTC DRUG
SPL set ID: e174f231-73df-464b-bd92-23222659df24
SPL ID: 3e84c52a-03fb-4630-9bed-0c230e5dc548
Version: 3
Effective date: 2026-07-21
Source export date: 2026-11-06
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:46:22

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		DOCTOR INKS HAND SANITIZER	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Enviro Specialty Chemicals Inc	openfda.manufacturer_name
ndc	package	71884-201-06	openfda.package_ndc
ndc	package	71884-201-04	openfda.package_ndc
ndc	package	71884-201-03	openfda.package_ndc
ndc	package	71884-201-05	openfda.package_ndc
ndc	package	71884-201-01	openfda.package_ndc
ndc	package	71884-201-02	openfda.package_ndc
ndc	product	71884-201	openfda.product_ndc
ndc11	package	71884020104	derived:openfda.package_ndc
ndc11	package	71884020105	derived:openfda.package_ndc
ndc11	package	71884020106	derived:openfda.package_ndc
ndc11	package	71884020103	derived:openfda.package_ndc
ndc11	package	71884020101	derived:openfda.package_ndc
ndc11	package	71884020102	derived:openfda.package_ndc
rxcui		1020365	openfda.rxcui
spl id		3e84c52a-03fb-4630-9bed-0c230e5dc548	id
spl set id		e174f231-73df-464b-bd92-23222659df24	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 develop and persist 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.