DOCTOR INKS HAND SANITIZER- benzalkonium chloride liquid 
Enviro Specialty Chemicals Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

DOCTOR INK'S HAND SANITIZER

Drug Facts

Active Ingredient:

Benzalkonium Chloride 0.13%

Purpose:

Antiseptic, Hand & Skin Sanitizer

Uses:

Hand Sanitizer to help decrease bacteria on the skin - Recommended for repeated use.

Warnings:

Do not freeze. For external use only. Do not use in ears, eyes or mouth.

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

Directions:

Apply liberally to the palms of the hands. Rub into skin until dry. Recommended for repeat use.

Inactive Ingredients:

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Laureth-4, Phenoxyethanol, Triethoxysilylpropyl Steardimonium chloride.

Questions?

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

Long-lasting, alcohol-free protection from germs

Formulated and enhanced with Zetrisil®

Kills 99.9% of Germs

Alcohol Free

Contains Soothing Aloe Vera

Fast-acting
15-Second Formula

Foaming Pump Top

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

FORMULATED IN THE USA

MADE IN CHINA

Packaging

sanitizerfoam

DOCTOR INKS HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71884-201
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
LAURETH-4 (UNII: 6HQ855798J)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71884-201-0158 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/01/2022
2NDC:71884-201-02118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/01/2022
3NDC:71884-201-03244 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/01/2022
4NDC:71884-201-04473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/01/2022
5NDC:71884-201-051182 mL in 1 BAG; Type 0: Not a Combination Product09/01/2022
6NDC:71884-201-063785 mL in 1 JUG; Type 0: Not a Combination Product09/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/01/2022
Labeler - Enviro Specialty Chemicals Inc (202621850)

Revised: 2/2023
Document Id: beb81b1a-b614-4b84-addb-812a37c1d7fd
Set id: e174f231-73df-464b-bd92-23222659df24
Version: 1
Effective Time: 20230214
 
Enviro Specialty Chemicals Inc