DOCTOR INKS TOPICAL ANTISEPTIC- benzalkonium chloride gel

DOCTOR INKS TOPICAL ANTISEPTIC by

Drug Labeling and Warnings

DOCTOR INKS TOPICAL ANTISEPTIC by is a Otc medication manufactured, distributed, or labeled by Enviro Specialty Chemicals Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts:

ACTIVE INGREDIENT:

Benzalkonium Chloride 0.13%

PURPOSE:

First aid antiseptic.
Topical skin treatment - Barrier Gel

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 

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.

DIRECTIONS:

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

INACTIVE INGREDIENTS:

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

QUESTIONS?

+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

INGREDIENTS AND APPEARANCE

DOCTOR INKS TOPICAL ANTISEPTIC 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71884-203
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
LAURETH-4 (UNII: 6HQ855798J)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71884-203-01	30 mL in 1 TUBE; Type 0: Not a Combination Product	09/01/2022
2	NDC: 71884-203-02	59 mL in 1 TUBE; Type 0: Not a Combination Product	09/01/2022
3	NDC: 71884-203-03	118 mL in 1 TUBE; Type 0: Not a Combination Product	09/01/2022
4	NDC: 71884-203-04	237 mL in 1 TUBE; Type 0: Not a Combination Product	09/01/2022
5	NDC: 71884-203-05	3785 mL in 1 JUG; Type 0: Not a Combination Product	09/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/01/2022

Labeler - Enviro Specialty Chemicals Inc (202621850)