DOCTOR INKS TOPICAL ANTISEPTIC - Enviro Specialty Chemicals Inc

Manufacturer: Enviro Specialty Chemicals Inc
Effective date: 2026-07-21
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: daily-update
Hydrated at: 2026-07-29 05:10:10

Label at a glance#

ProductDOCTOR INKS TOPICAL ANTISEPTIC

Active ingredientBENZALKONIUM CHLORIDE

Label structure9 sections

Indications and uses

First aid soothing relief, reduced skin drying of newly applied tattoos, piercings, and germ protection for minor cuts, scrapes, burns, skin irritations and minor abrasions

Dosage and administration

Apply liberally over new Tattoo artwork or piercings, recommended for repeat application regularly.

Contacts and useful links#

PhoneLabel contact+1(888) 331-8332

Websitewww.doctorink.com

www.doctorink.com

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

PURPOSE:

OTC - PURPOSE SECTION

First aid antiseptic.
Topical skin treatment - Barrier Gel

Uses:

INDICATIONS & USAGE SECTION

First aid soothing relief, reduced skin drying of newly applied tattoos, piercings, and germ protection for minor cuts, scrapes, burns, skin irritations and minor abrasions

WARNINGS:

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Children should be supervised when using this product.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Apply liberally over new Tattoo artwork or piercings, recommended for repeat application regularly.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Aloe barbadensis leaf extract, aqua, laureth-4, citric acid, hydroxyethyl cellulose, phenoxyethanol, triethoxysilylpropyl Steardimonium chloride.

QUESTIONS?

OTC - QUESTIONS SECTION

+1(888) 331-8332, M-F, 9AM-5PM (EST)

SPL UNCLASSIFIED SECTION

Alcohol-Free

Long lasting, soothing protection from germs.

KILLS 99.9% OF GERMS

Formulated and enhanced with Zetrisil^®

Contains Soothing Aloe Vera

Fast-acting
15-second Formula

DISTRIBUTED BY:
ESC Brands, LLC.
1060 Blue Prince Road
Bluefield, WV 24701
www.doctorink.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antisepticgel-203

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

DOCTOR INKS TOPICAL ANTISEPTIC
Benzalkonium Chloride
BENZALKONIUM
ALOE VERA LEAF
WATER
LAURETH-4
CITRIC ACID MONOHYDRATE
HYDROXYETHYL CELLULOSE, UNSPECIFIED
PHENOXYETHANOL
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71884-203	71884-203-01, 71884-203-02, 71884-203-03, 71884-203-04, 71884-203-05

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
ALOE VERA LEAF	ZY81Z83H0X	IACT
WATER	059QF0KO0R	IACT
LAURETH-4	6HQ855798J	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
HYDROXYETHYL CELLULOSE, UNSPECIFIED	T4V6TWG28D	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE	XGN40YQC7B	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
2	2024-12-23	full-release	2026-06-01 00:50:47

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DOCTOR INKS TOPICAL ANTISEPTIC	BENZALKONIUM CHLORIDE	Enviro Specialty Chemicals Inc	d503a2db-e326-4a31-bc6a-5034ad74bf0b	2026-07-21	Warnings	Exact identifier ndc (package): 71884-203-03 ndc (package): 71884-203-01 ndc (package): 71884-203-04 ndc (package): 71884-203-02 ndc (package): 71884-203-05 ndc (product): 71884-203 ndc11 (package): 71884020303 ndc11 (package): 71884020304 ndc11 (package): 71884020305 ndc11 (package): 71884020301 ndc11 (package): 71884020302 spl id: 1984543f-4ded-41ba-acf8-5e3813680672 spl set id: d503a2db-e326-4a31-bc6a-5034ad74bf0b

Reported adverse events (FAERS/openFDA)#

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