Consult Health Persistence Hand Sanitizer

Manufacturer
Geo Management Corporation | Great American Emu Company, LLC
Effective date
2021-07-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:41:39

Label at a glance#

ProductConsult Health Persistence Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin.  Recommended for repated use. For wound sanitizing to help preven bacterial contamination in cuts, scrapes, burns, lacerations and skin infections.

Dosage and administration

Pump onto hands as needed.  Rub briskly together until dry.  No rinsing required. Pump onto wounds 3 times a day after cleaning.  Allow foam to dissipate.  Wipe excess with sterile gauze.  May be bandaged once dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial and First aid antiseptic

Uses:

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the skin.  Recommended for repated use.
  • For wound sanitizing to help preven bacterial contamination in cuts, scrapes, burns, lacerations and skin infections.

Warnings:

WARNINGS SECTION

For External Use Only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes.  In case of eye contacct, flush eyes with water.

Discontinue use

OTC - STOP USE SECTION

if irritation or redness develops.  If condition persists for more than 72 hours consult doctor.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get immediate help or contact a poison control center right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Pump onto hands as needed.  Rub briskly together until dry.  No rinsing required.
  • Pump onto wounds 3 times a day after cleaning.  Allow foam to dissipate.  Wipe excess with sterile gauze.  May be bandaged once dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

ionized water, carbamide

​Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70803-002-072023-01-30C16284748780-1f386c64a-0d42-0266-e053-dadaa90a7c1aConsult Health Persistence Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70803-002-07Consult Health Persistence Hand Sanitizer210 mL in 1 BOTTLE, PUMPCREAM2103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70803-002CONSULT HEALTH PERSISTENCE HAND SANITIZER (BENZALKONIUM CHLORIDE) CREAM [GEO MANAGEMENT CORPORATION]3Legacy NDC, 1 package rows20210724_ef051c3c-5d04-41a7-8a27-81a5cd88e8ea.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70803-00270803-002-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
UREA8W8T17847WIACT
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
c7d1c12c-2aec-4d28-e053-2a95a90a4966ef051c3c-5d04-41a7-8a27-81a5cd88e8ea2021-07-23WarningsExact identifier
spl id: c7d1c12c-2aec-4d28-e053-2a95a90a4966
spl set id: ef051c3c-5d04-41a7-8a27-81a5cd88e8ea

Reported adverse events (FAERS/openFDA)#

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