FDA.reportPublic FDA data

CURX Hand Sanitizer

Manufacturer
Global Health Solutions DBA Turn Therapeutics | Westwood Labs, Inc.
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:17:18

Label at a glance#

ProductCURX Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

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

Dosage and administration

spray a small amount of liquid into palm of both hand rub thoroughly over all the surfaces of both hands rub hands together briskly until dry

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Benzalkonium Chloride 0.13%

Drug Facts

OTC - PURPOSE SECTION

Purpose

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

  • spray a small amount of liquid into palm of both hand
  • rub thoroughly over all the surfaces of both hands
  • rub hands together briskly until dry

Inactive Ingredients

INACTIVE INGREDIENT SECTION

water, didecyldimonium chloride, propylene glycol, methylparaben, diazolidinyl urea, propylparaben, cocamidopropylamine oxide, allantoin, cocamidopropyl betaine, cetrimonium chloride, triethanolamine, citric acid

POWERED BY CURX®

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

anti-microbial

HAND SANITIZER

Kills 99% of

GERMS

Distributed By:

Nail Alliance - North America, Inc.

1545 Moonstone

Brea, CA 92821

CURXCURX

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69578-46469578-464-08, 69578-464-99

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
METHYLPARABENA2I8C7HI9TIACT
PROPYLPARABENZ8IX2SC1OHIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
ALLANTOIN344S277G0ZIACT
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
2,2'-((2-(DODECYLOXY)ETHYL)IMINO)BISETHANOL5MYL465X9VIACT
COCAMIDOPROPYLAMINE OXIDEM4SL82J7HKIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ed16be20-48f0-6ecd-e053-2995a90a5162a3aecd69-4e2b-0ed2-e053-2995a90ad4ee2022-11-09WarningsExact identifier
spl set id: a3aecd69-4e2b-0ed2-e053-2995a90ad4ee

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.