Pure + Dew Hand Sanitizer

Pure Dew Hand Sanitizer by

Drug Labeling and Warnings

Pure Dew Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by HOME & BODY COMPANY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURE DEW HAND SANITIZER- benzalkonium chloride liquid 
HOME & BODY COMPANY

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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Pure + Dew Hand Sanitizer

Active ingredient

0.13% Benzalkonium Chloride

Purpose

Antibacterial

Use

Helps reduce bacterial on the skin

Warning

For external use only.
When using this product do not use in or near the eyes.
In case of contact, rinse eyes throughly with water.

Keep out of reach of children

Keep out of reach of children, except under adult supervision. If swallowed, get medical help or
contact a Poison Control Center right away.

Directions

Place enough product in your palm to throughly cover hands. Rub hands together briskly until dry

Inactive Ingredients

Fragrance, Glycerin, Isopropyl Alcohol, Polysorbate 20, Water (Aqua)

Product Label

label

PURE DEW HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73746-045
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
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73746-045-0159 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/06/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/06/202010/05/2022
Labeler - HOME & BODY COMPANY (081290720)
Registrant - HOME & BODY COMPANY (081290720)
Establishment
NameAddressID/FEIBusiness Operations
HOME & BODY COMPANY081290720api manufacture(73746-045)

Revised: 10/2022
Document Id: ea61cc9e-6ed0-3b50-e053-2995a90a1826
Set id: b1041f56-4dd8-99b5-e053-2995a90a3583
Version: 6
Effective Time: 20221006