DOCTOR INKS SANITIZING- benzalkonium chloride soap

DOCTOR INKS SANITIZING by

Drug Labeling and Warnings

DOCTOR INKS SANITIZING 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 0.10%

Purpose:

Antiseptic Hand Soap

Uses:

• Hand wash to help reduce bacteria that potentially can cause disease
• Helps to prevent cross-contamination by hand contact
• Helps to prevent drying of skin Recommended for repeat use

Warnings:

• For external use only
• When using this product do not use in or near eyes
• Stop use and ask doctor if irritation and redness develop

• Keep out of reach of children,
• If swallowed, seek medical attention or contact a Poison Control Center immediately.

STORAGE AND HANDLING

Store in a cool dry place below 104° F (40°C)

Directions:

Wet hands and wrists with clean running water
Apply appropriate amount of product
Lather & scrub hands, fingers, fingernails, cuticles & wrists thoroughly
Rinse thoroughly with running water
Dry hands completely (incomplete drying may result in chapped skin)

Inactive Ingredients:

Aloe Barbadensis Leaf Juice, Aqua, Benzyl Alcohol, Citric Acid, Glycerin, Lauramidopropyl Betaine, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

Questions?

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

SPL UNCLASSIFIED SECTION

FDA Registered Anti-Microbial Soap for cleaning grime and germs from your hands

Kills 99.9% of Germs

Formulated and enhanced with Zetrisil®

Alcohol Free

Contains Soothing Aloe Vera

Fast-acting
15-Second Formula

Foaming Pump Top

FORMULATED IN THE USA

MADE IN CHINA

Distributed by:
ESC Brands, LLC.
1060 Blue Prince Road
Bluefield, WV 24701
www.doctor-ink.com

Packaging

INGREDIENTS AND APPEARANCE

DOCTOR INKS SANITIZING 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71884-200
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71884-200-01	118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/30/2022
2	NDC: 71884-200-02	244 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/30/2022
3	NDC: 71884-200-03	473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/30/2022
4	NDC: 71884-200-04	1182 mL in 1 BAG; Type 0: Not a Combination Product	06/30/2022
5	NDC: 71884-200-05	3785 mL in 1 JUG; Type 0: Not a Combination Product	06/30/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/30/2022

Labeler - Enviro Specialty Chemicals Inc (202621850)