DEWZI ALCOHOL FREE HAND SANITIZER FRAGRANCE FREE- benzalkonium chloride liquid 
LAB-CLEAN, 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.

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Active ingredient

Benzalkonium Chloride  0.1%

Purpose

Antimicrobial

Uses

For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.

Warnings

For external use only.

When using this product, avoid contact with eyes. In case of eye contact flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or  contact a Poison Control Center right away.

Directions

Inactive ingredients

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocoate, Citric Acid

Product label

image description

DEWZI ALCOHOL FREE HAND SANITIZER FRAGRANCE FREE 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73126-031
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73126-031-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product02/10/2021
2NDC:73126-031-0288 mL in 1 BOTTLE; Type 0: Not a Combination Product02/10/2021
3NDC:73126-031-03236 mL in 1 BOTTLE; Type 0: Not a Combination Product02/10/2021
4NDC:73126-031-04355 mL in 1 BOTTLE; Type 0: Not a Combination Product02/10/2021
5NDC:73126-031-05474 mL in 1 BOTTLE; Type 0: Not a Combination Product02/10/2021
6NDC:73126-031-06710 mL in 1 PACKAGE; Type 0: Not a Combination Product02/10/2021
7NDC:73126-031-07946 mL in 1 PACKAGE; Type 0: Not a Combination Product02/10/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/10/202104/20/2024
Labeler - LAB-CLEAN, INC (199822219)
Establishment
NameAddressID/FEIBusiness Operations
LAB-CLEAN, INC199822219manufacture(73126-031)

Revised: 4/2022
Document Id: dd944506-1dab-402b-e053-2a95a90a3430
Set id: 3bd749fd-d1e9-4f2d-bf6b-d659e673c73a
Version: 2
Effective Time: 20220426
 
LAB-CLEAN, INC