DOCTOR INK TOPICAL ANTISEPTIC WITH PAIN RELIEF - 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 05:10:14

Label at a glance#

ProductDOCTOR INK TOPICAL ANTISEPTIC WITH PAIN RELIEF
Active ingredientBENZALKONIUM CHLORIDE, LIDOCAINE
Label structure9 sections

Indications and uses

First aid pain relief, soothing, reduced drying of newly applied Tattoo or piercings and germ protection for: tattoos, piercings, 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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%, Lidocaine 4.0%

PURPOSE:

OTC - PURPOSE SECTION

First aid antiseptic, Topical skin treatment, Barrier gel with mild pain relief

Uses:

INDICATIONS & USAGE SECTION

First aid pain relief, soothing, reduced drying of newly applied Tattoo or piercings and germ protection for: tattoos, piercings, 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 Lidocaine + 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

PainReliefGel-204PainReliefGel-204

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71884-20471884-204-01, 71884-204-02, 71884-204-03, 71884-204-04, 71884-204-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-12-31full-release2026-06-01 00:50:48

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DOCTOR INK TOPICAL ANTISEPTIC WITH PAIN RELIEFBENZALKONIUM CHLORIDE, LIDOCAINEEnviro Specialty Chemicals Incf7abe66c-dc2d-4ef7-9b11-5b87157fd3022026-07-21WarningsExact identifier
ndc (package): 71884-204-04
ndc (package): 71884-204-03
ndc (package): 71884-204-01
ndc (package): 71884-204-05
ndc (package): 71884-204-02
ndc (product): 71884-204
ndc11 (package): 71884020404
ndc11 (package): 71884020403
ndc11 (package): 71884020405
ndc11 (package): 71884020402
ndc11 (package): 71884020401
spl id: 09dd7a4a-1a4a-4237-b72c-6ed735c73c36
spl set id: f7abe66c-dc2d-4ef7-9b11-5b87157fd302

Reported adverse events (FAERS/openFDA)#

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